Le Diko - en:increased serum lactate, particularly after exercise

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Le Diko - en:increased serum lactate, particularly after exercise

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le dictionnaire d'associations lexicales
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en:increased serum lactate, particularly after exercise

Nom

Informations lexicales

Langue:anglais

Associations d'idées

1000

Maladie de Tay-Sachs

•

en:decreased activities of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acid dehydrogenase complex

•

en:decreased mucosal alkaline phosphatase

•

en:decreased activity of 2-methyl-3-hydroxybutyryl co-a dehydrogenase

•

en:decreased or absent apolipoprotein a-i

•

en:decreased b cells

•

en:inappropriately normal serum 1,25-dihydroxyvitamin d3

•

en:decreased mitochondrial nadp(h)

•

en:high urinary excretion of inosine, 2'deoxyinosine, guanosine, and 2'deoxyguanosine

•

en:decreased serum iga

•

en:decreased serum factor i (atypical hus)

•

en:alkaline phosphatase normal

•

en:continuous urinary iodine loss

•

en:high serum inosine levels

•

en:abnormal secretin test

•

en:decreased fbp1 enzyme activity

•

en:absent/reduced free proteins and absent total protein s

•

en:decreased phosphoglycerate mutase 1 (pgam2) activity (2 to 6% of normal values)

•

en:fluorescence in situ hybridization specific probe for mds critical region

•

en:elevated alkaline phosphatase (varies from 1.3-20 times age-adjusted upper limit of normal)

•

en:hyperkalemia (7.5 +/- 0.9 mm)

•

en:hepatic carbamoylphosphate synthetase i deficiency

•

en:fibroblasts accumulate dol-pp-glcnac2man5

•

en:granular osmiophilic cytoplasmic deposits ultrastructurally in cells

•

en:glycoamino aciduria

•

en:elevated urinary and csf ribitol and d-arabitol

•

en:elevated plasma ammonia

•

en:deficiency of prolidase activity in erythrocytes, leukocytes, or fibroblasts

•

en:elevated hdl (2-6x normal) in homozygotes

•

en:decreased acid sphingomyelinase activity

•

en:elevated 1,25(oh)2 d3

•

en:decreased activity of mitochondrial respiratory complexes

•

en:hypogammaglobulinemia, profound

•

en:electron microscopy of patient respiratory cells shows loss of ciliary outer dynein arms

•

en:abnormal serum lipoprotein levels (in 3 of 10 patients)

•

en:abnormal transaminases (1 patient)

•

en:elevated serum glutamic pyruvic transaminase (sgpt)

•

en:alpha fetoprotein increased

•

en:decreased von willebrand factor

•

en:decreased serum ceruloplasmin

•

en:decreased glutamine in bodily fluids

•

en:decreased homovanillic acid (hva) and 5-hydroxyindoleacetic acid (5hiaa) in csf

•

en:decreased adiponectin

•

en:decreased atp synthase in muscle, heart, liver, and brain

•

en:hypogammaglobulinemia

•

en:decreased activity of thymidine phosphorylase

•

en:transaminitis

•

en:increased ige level

•

en:cystathionine beta-synthase deficiency disease

•

en:transcobalamin ii deficiency

•

en:glycogen storage disease type vi

•

déficit en biotinidase

•

en:ballooned neurons

•

en:decreased levels of csf hypocretin (hcrt, 602358)

•

en:3-methylglutaconic aciduria

•

en:hypoproteinemia (in 1 patient)

•

en:aldolase a deficiency

•

en:abnormal liver enzymes (rare)

•

en:hypoprebetalipoproteinemia

•

en:acetylcholinesterase staining reveals nerve trunk hypertrophy

•

en:elevated urinary pge(2) levels

•

en:histiocytic infiltration of liver, spleen, and lungs

•

en:decreased activity of galactocerebrosidase

•

en:detection by rt-pcr and southern blot analysis for primary diagnosis and follow up for residual disease

•

en:granular osmiophilic deposits (grod) in cells resulting in 'fingerprint' profiles ultrastructurally

•

en:decreased t cells

•

en:elevated fibroblast free sialic acid

•

en:decreased number of igf1 receptors (igf1r, 147370) on cell surface

•

en:elevated plasma alloisoleucine

•

en:decreased beta-galactosidase activity

•

en:hyperkalemia (5.8 +/- 0.8 mm)

•

en:decreased acid beta galactosidase protein and activity

•

en:hyperbilirubinemia in those with liver failure

•

en:increased ck-mb

•

en:intermittent increase of urinary ethylmalonic acid

•

en:increased thymine and dihydrothymine in bodily fluids

•

en:increased serum thrombopoietin may occur

•

en:low serum magnesium

•

en:marked elevation of erythrocyte sedimentation rate

•

en:low or absent thyrotropin (tsh)

•

en:low to normal tsh (values may vary depending on the measurement methods used)

•

en:elevated liver enzymes during episodes

•

en:karyomegaly may be found in other visceral organs

•

en:increased serum alpha-mannosidase

•

en:lacunar halos around chondrocytes in skeletal cartilage

•

en:inclusion bodies (membrane-bound vacuoles) in fibroblasts

•

en:liver phosphorylase kinase (phk) deficiency

•

en:increased plasma phytanic acid

•

en:absence of protein-bound lipoic acid

•

coagulopathie intravasculaire disséminée

•

en:increased csf protein during acute illness

•

réparation défectueuse de l'ADN

•

en:deficiency of serum properdin p factor

•

•

maladie de Tay-Sachs

•

hypo-albuminémie

•

Coagulopathie intravasculaire disséminée

•

maladie de Tay-sachs

•

•

•

en:hyperlipemia

•

•

en:serum bicarbonate increased

•

en:parathyroid hormone level increased

•

en:abetalipoproteinemia

•

en:plasma aldosterone normal

•

en:intermittent 3-methylglutaconic aciduria

•

en:hyperlipoproteinemia

•

en:low alkaline phosphatase

•

en:elevated resting serum lactate, increased with exercise

•

en:hyposthenuria (inability to concentrate urine normally)

•

en:glcnac-transferase ii deficiency in fibroblast and mononuclear cells

•

en:galactosyltransferase i deficiency in fibroblasts

•

en:hyperkalemia (>6.2 mm in both dominant and recessive)

•

en:hypermethioninemia, progressive

•

en:fibroblasts show lamellar lysosomal inclusions on electron microscopy

•

en:hyperchloremia (mean 111 mm)

•

en:howell-jolly bodies seen in peripheral blood smear

•

en:glycogen accumulation in both liver and muscle

•

en:hyperkalemia during attacks

•

en:decreased ubiquinone-10

•

en:hyperbilirubinemia, unconjugated, 20-30mg/dl

•

en:decreased serum carnitine in acute stage

•

en:increased serum beta-hexosaminidase

•

en:elevated afp (endodermal sinus tumor)

•

en:fingerprint intracellular accumulation of autofluorescent lipopigment storage material

•

en:elevated sweat chloride

•

en:increased serum erythropoietin (epo, 133170)

•

en:increased urinary 7-biopterin (primapterin)

•

en:increased serum 18-hydroxycorticosterone (18-ohb)

•

en:increased urinary succinic acid

•

en:lack of lysosomal inclusions in visceral organs

•

en:increased urinary, plasma, and csf dihydrothymine

•

en:increased excretion of urobilinogen

•

en:increased urinary porphyrin precursors porphobilinogen (pbg) and delta-aminolevulinic acid (ala) during acute attacks

•

en:increased alpha-fetoprotein in the mother during early pregnancy while carrying an affected fetus

•

en:decreased platelet derived growth factor

•

en:decreased plasma lysine, glutamic acid, and glutamine

•

en:breastfed offspring have transient decrease of plasma zinc levels

•

en:elevated urinary 7 alpha-hydroxylated bile alcohols

•

en:fibroblasts show decreased mitochondrial complex v activity

•

en:creatine phosphokinase serum increased

•

en:galactosylation defects

•

en:abnormal liver enzymes, intermittent (1 patient)

•

en:decreased iga, igg, igm

•

en:decreased csf arginine

•

en:decreased levels of coenzyme q10 in skeletal muscle (5-35%)

•

en:chromosomal instability

•

en:decreased activity of mitochondrial respiratory complexes i, iii, and iv

•

en:absent igg2 subclass

•

en:heparin cofactor ii deficiency (disorder)

•

en:elevated erythrocyte sedimentation rate (mean 90mm/h)

•

en:cilia may also be static, with slow activity

•

en:decreased serum insulin-like growth factor-1 (igf1, 147440)

•

en:elevated serum levels of follicle stimulating hormone (fsh)

•

en:hypofibrinogenemia

•

en:acylglycinuria

•

en:fatty acid pattern of serum lecithin shows increased arachidonic acid and decreased linoleic acid

•

en:cd4+/cd8+ ratio often reversed

•

en:decreased phgdh activity (fibroblasts)

•

en:creatine kinase levels may normalize with disease progression

•

en:3-methylglutaric aciduria

•

en:electroretinogram is abnormal--rod responses are mildly abnormal and cone responses are markedly diminished

•

en:decreased testosterone level

•

en:high nonceruloplasmin-bound serum copper

•

en:decreased tissue and serum alkaline phosphatase

•

en:decreased csf methyltetrahydrofolate (mthf)

•

en:anti-ssb positive

•

en:cellular arrest at g2 of the cell cycle

•

en:decreased telomerase activity

•

en:decreased or normal serum c3

•

en:decreased serum 18-ohb

•

en:decreased levels of the e2 subunit protein

•

en:fibroblasts show increased sensitivity to apoptosis

•

en:decreased cytochrome c oxidase activity in skin fibroblasts, liver, and skeletal muscle

•

en:delta-1-pyrroline-5-carboxylate (p5c) levels increased in plasma

•

en:cytogenetic deletion of chromosome 17p13.3

•

en:hyperbilirubinemia, non-hemolytic unconjugated (may rise with fasting or dehydration)

•

en:hypoglycemia, fasting

•

en:decreased activity of aromatic l-amino acid decarboxylase (aadc)

•

en:cell studies show increased dna breakage

•

en:abnormal n-glycosylation of transferrin

•

en:abnormally low cerebrospinal fluid cystatin c

•

en:xanthine nephrolithiasis

•

en:thyroid dyshormonogenesis 5

•

en:infantile hypophosphatasia

•

en:decreased blood levels of cationic amino acids

•

en:hereditary fructose intolerance

•

en:hyperinsulinemic hypoglycemia, familial, 7

•

en:hyperlysinemia

•

en:hypercalciuria

•

en:1,25-dihydroxyvitamin d was elevated in childhood but deficient in adulthood

•

en:chromosome inversion - inv2(p12q14) in 2 patients

•

en:decreased grhpr activity

•

en:decreased csf homovanillic acid (hva)

•

en:abetalipoproteinemia (lab finding)

•

en:folic acid deficiency

•

en:decreased tissue total and free carnitine

•

en:high resolution g- and t- banding karyotype shows reciprocal translocation of distal 9p-6q

•

en:decreased serum follicle-stimulating hormone (fsh)

•

en:elevated ast and ldh, especially infantile-onset

•

en:deficiency or absence of cytochrome b(-245)

•

en:fibroblasts show global defects in multiple mitochondrial respiratory chain activities

•

en:generalized aminoaciduria

•

en:decreased or absent alpha-n-acetylgalactosaminidase protein

•

en:fumarase deficiency

•

en:decreased serum rt3

•

en:elevated dihydrobiopterin in csf

•

en:decreased long-chain fatty acid oxidation

•

en:decreased mitochondrial complex v assembly

•

en:decreased fibroblast arylsulfatase a

•

en:decreased phosphoglucomutase 1 (pgm1) activity (less than 10% of normal values)

•

en:excretion of dermatan sulfate and heparan sulfate in urine

•

en:hypercalciuria (in childhood)

•

en:disorganized growth plate cartilage

•

en:low rai (radioactive iodine) uptake

•

en:increased urinary excretion of coproporphyrin i

•

en:increased serum pyruvate in acute stage

•

en:increased 18-oxocortisol

•

en:increased urinary delta-aminolevulinic acid (ala) and porphobilinogen (pbg) during acute attacks

•

en:increased serum lactate dehydrogenase (ldh)

•

en:low serum igg and iga

•

en:marked hypoalphalipoproteinemia (in some patients)

•

en:mean platelet volume (mpv) 12.6fl

•

en:low plasma triglyceride level

•

en:keratan sulfaturia in some patients

•

en:low-molecular-weight proteinuria

•

en:increased biopterin in urine and csf

•

en:increased urinary carnitine

•

en:avitaminosis D

•

en:increased urinary homovanillic acid (hva)

•

•

en:increased urinary uracil

•

déficit en prolidase

•

en:elevated plasma insulin

•

mucolipidose II

•

•

intolérance au fructose

•

•

hypoalbuminémie

•

en:hemophilia B

•

en:decreased hdl cholesterol

•

•

•

en:serum iron normal

•

en:raised tsh level

•

en:elevated serum very long chain fatty acids (vlcfa)

•

en:hyponatremia

•

en:double stranded anti dna antibody

•

en:keratan sulfate excretion in urine that decreases with age

•

en:increased d-glyceric acid in serum, urine, and csf

•

en:increased serum c-reactive protein, episodic

•

en:hypophosphatemia (less common)

•

en:impaired oxidation of pyruvate

•

en:hypomethylation of satellite repeats on chromosome 1, 9, and 16

•

en:high plasma citrulline (1000-5000 micromolar)

•

en:elevated bilirubin (bilirubinemia)

•

en:hyponatremia in infancy

•

en:hyperphosphatemia, transient

•

en:decreased serum factor h (atypical hus)

•

en:high deoxypyridinoline/creatinine (in some patients)

•

en:fibroblasts show elongated, tangled, tubular mitochondria

•

en:excessive urinary 5-oxo-l-proline

•

en:elevated fasting glucose

•

en:fibroblasts have decreased levels of ceramide, sphingomyelin, lactosylceramide, ceramide trihexoside, and globoside

•

en:homocitrullinuria

•

en:elevated ast (aspartate aminotransferase) and cpk (creatine phosphokinase)

•

en:increased urinary o-hydroxyphenylacetic acid, phenylpyruvic acid, phenylacetic acid and phenylacetylglutamine

•

en:decreased mitochondrial respiratory complexes i, iii, and iv in brain, heart, and skeletal muscle

•

en:hyperphenylalaninemia

•

en:homocystinuria (in some patients)

•

en:increased ferritin

•

en:intermittent ethylmalonic aciduria

•

en:increased pyruvate in serum and csf

•

en:increased creatine kinase, mild to moderate

•

en:increased serum ige

•

en:low copper and ceruloplasmin

•

en:increased serum alpha-interferon (ifna1, 147660)

•

en:low or low-normal serum t4

•

en:increased csf, plasma, and urinary l-dopa

•

en:increased osmotic fragility

•

en:elevated urinary free sialic acid (n-acetylneuraminic acid)

•

en:deletion (78kb to 1mb) of chromosome 8q24.3 including the scrib (607733) and puf60 (604819) genes

•

en:elevated alkaline phosphatase (if more than one affected site)

•

en:immediate (type i) skin test reactivity

•

en:chromosomal translocations involving c-myc (190080, 8q24) and the immunoglobin lambda light chain (147220, 22q11.2) locus

•

en:inactive mutant form of red cell carbonic anhydrase b in one sibship

•

en:abnormal isoelectric focusing of serum transferrin

•

en:aminoaciduria, intermittent

•

en:4-hydroxycyclohexylacetic aciduria (adults)

•

en:elevated 8(9)-cholestenol

•

en:hyperglycinemia (1 patient)

•

en:igg, decreased

•

en:elevated plasma estrogen

•

en:fibroblasts show decreased peroxisomes arranged in rows

•

en:decreased tetrahydrobiopterin (bh4) in csf

•

en:decreased free t(3)/free t(4)

•

en:fibronectin decreased

•

en:deficiency of glycoprotein (gp)iib-iiia complex

•

en:foam cells contain polymorphic cytoplasmic inclusions consisting of lamellar osmiophilic membranes on electron microscopy

•

en:decreased insulin receptor binding

•

en:abnormal urinary oligosaccharides

•

en:abnormal liver function tests (in some patients)

•

en:decreased or absent serum citrulline

•

en:2-aminoadipic aciduria

•

en:decreased c3 antigen

•

en:elevated plasma and urine inorganic pyrophosphate (ppi)

•

en:decreased urocanic acid in blood, urine, and skin cells

•

•

en:hypokalemia during periodic paralysis (most patients)

•

en:decreased activity of the pyruvate dehydrogenase (pdh) complex

•

en:decreased serum bun

•

en:decreased renal calcium excretion

•

en:hair bulb tyrosinase present

•

en:immunoreactive pc protein

•

en:gaucher cells, diffuse, in spleen, liver, lymph nodes, bone marrow, central nervous system

•

en:decreased serum c3 (atypical hus)

•

en:abnormal karyotype in 3 patients involving distal 6p

•

en:abnormal nasal potential difference

•

en:decreased coproporphyrinogen oxidase activity (hcp, lymphocytes, 50% of normal)

•

en:abacterial leukocyturia

•

en:hyperbilirubinemia, unconjugated, <20mg/dl

•

en:dimethylglycine dehydrogenase (dmgdh) deficiency

•

en:microscopic hematuria

•

en:decreased urinary sulfate

•

•

en:accumulation of unprocessed mt-trna intermediates in skeletal muscle cells and fibroblasts

•

en:reticulocytosis

•

en:farber lipogranulomatosis

•

en:indirect bilirubin increased

•

en:serum transaminase increased

•

en:hyperammonemia

•

en:lactate dehydrogenase increased

•

en:glycogen storage disease type vii

•

en:associated with serum anti-phospholipid antibodies in about 50% of patients

•

en:hawkinsinuria

•

en:methylmalonyl-coenzyme a mutase deficiency

•

en:hemophilia b

•

en:hyperprolinemia type 1

•

en:decreased serum leptin

•

en:hyperoxalaemia

•

en:'compensated hypothyroidism' with increased tsh and normal t4

•

en:abnormal serum glycoproteins

•

en:decreased activity of long-chain 3-hydroxyacyl-coa dehydrogenase, long-chain 3-oxoacyl-coa thiolase, and long-chain 2-enoyl-coa hydratase

•

en:decreased activity of the pdh phosphatase

•

en:decreased serum alpha-2 macroglobulin levels

•

en:glutathione deficiency

•

en:elevated urinary delta-aminolevulinic acid

•

en:decreased plasminogen antigen

•

en:elevated acth

•

en:decreased levels of serum vitamin b12

•

en:decreased arylsulfatase a (arsa) activity in urine, leukocytes, fibroblasts

•

en:anti-ds dna antibody

•

en:decreased nk cells (in some patients)

•

en:3-methylglutaconic aciduria (3-mgc)

•

en:abnormal dystrophin on muscle biopsy

•

en:cystathioninuria (lab finding)

•

en:d-2-hydroxyglutaric aciduria

•

en:decreased fibrinogen (in some patients)

•

en:curvilinear intracellular accumulation of autofluorescent lipopigment storage material

•

en:decreased clot retraction

•

en:decreased csf tetrahydrofolate and 5-methyltetrahydrofolate

•

en:decreased circulating aldosterone level

•

en:bile shows increased cholesterol/phospholipid ratio

•

en:decreased cholesterol (less common)

•

en:increased tissue levels of free fatty acids

•

hypophosphatasie infantile

•

hypophosphatasie foetale

•

en:increased triglycerides (less common)

•

en:marked hypobetalipoproteinemia

•

en:increased serum plasminogen activator inhibitor-1 (pai1, 173360)

•

en:increased urinary ketones

•

en:increased succinyladenosine (s-ado) in serum, urine, and csf

•

en:increased serum and csf lactate

•

en:increased serum bilirubin due to hemolysis

•

en:low or absent iga levels

•

en:increased urinary cyclic amp (camp) in response to ddavp administration

•

en:low serum alpha-fetoprotein (recessive)

•

en:increased csf and plasma ghb

•

en:increased serum lipoproteins

•

en:increased plasma long-chain acylcarnitines

•

en:intracellular glycosphingolipid deposition in all tissues of the body

•

en:median mean platelet volume (mpv) 18fl

•

•

en:increased urinary excretion of cystine

•

en:increased urinary hga

•

en:hyperlipaemia

•

•

hypo-intense (signal IRM)

•

en:glomerular filtration rate decreased

•

agrégation plaquettaire sai diminuée

•

en:positive antinuclear antibody test

•

en:decreased activity of mitochondrial complex i

•

en:increased serum unconjugated bilirubin

•

en:low or undetectable insulin

•

en:increased plasma pristanic acid

•

en:increased serum vitamin b12

•

en:increased urinary glycerol

•

en:increased uracil and dihydrouracil in bodily fluids

•

en:low fasting glucose (in some patients)

•

en:low or absent follicle stimulating hormone (fsh)

•

en:markedly increased serum creatine kinase

•

en:increased bile acid intermediates (dhca and thca)

•

en:impairment of urinary concentration

•

en:isochromosome often missing in lymphocyte

•

en:cortisol does not decrease on dexamethasone suppression test

•

en:decreased axonal flare response after intradermal histamine injection

•

en:hair bulbs will pigment when incubated with tyrosine

•

en:hypoglycorrhachia (low glucose in csf)

•

en:elevated plasma desmosterol

•

en:exercise-induced myoglobinuria in adults

•

en:elevated serum alkaline phosphatase during hyperplastic callus formation

•

en:granular osmiophilic deposits (grod) in cells resulting in 'rectilinear' profiles ultrastructurally

•

en:decreased levels of plasma factor viii

•

en:decreased urinary hva, 5-hiaa, and vanillyl mandelic acid (vma)

•

en:hemizygous deletion at 4p16.3

•

en:c-band karyotype shows 'railroad track' appearance

•

en:elevated 8-dehydrocholesterol

•

en:elevated urinary ornithine, lysine, arginine

•

en:defect in double-stranded dna repair

•

en:diagnosis by exposing muscle biopsy to caffeine and/or halothane

•

en:increased serum lactate during metabolic crisis

•

en:gaucher disease, type 1

•

en:elevated serum parathyroid hormone (pth) level

•

en:elevated urinary mevalonic acid

•

en:high urinary copper

•

en:aminoaciduria (less common)

•

en:increased serum serotonin in 25%

•

en:increased frequency of premature centromere disjunction (pcd) in cultured fibroblasts, esp. chromosome 3

•

en:nonketotic hypoglycemia

•

en:decreased apoa-i and apoa-ii

•

en:high-normal plasma triglyceride concentration (in heterozygotes)

•

en:increased fractional excretion of urate (greater than 50%)

•

en:resistance to activated protein c due to factor v leiden

•

en:elevated urinary 3-methylglutaconate

•

en:hypercholesterolemia (10%)

•

en:hematuria, macroscopic and microscopic

•

en:elevated plasma adrenocorticotropic hormone (acth)

•

en:increased il-6

•

en:elevated sepiapterin in csf

•

en:hepatic ornithine transcarbamylase deficiency

•

•

en:extremely low creatine excretion

•

en:decreased serum insulin-like growth factor-1 (igf1)

•

en:decreased hepatic udp-glucuronyl-transferase activity

•

en:elevated serum insulin-to-c-peptide ratio

•

•

en:laboratory abnormalities

•

en:decreased activity of pyruvate dehydrogenase complex

•

en:antineutrophil antibody positivity

•

en:decreased beta-glucocerebrosidase protein and activity

•

en:hypocalcemia (64% of adults)

•

en:decreased activity of the e2 subunit (lipoyl transacetylase, 608770) of the pdh

•

en:high m-component

•

en:antiphospholipid antibody

•

en:elevated serum angiotensin-converting enzyme (ace)

•

en:hyperprolinemia (10-15 times normal)

•

en:hypercholesterolemia, 350-550 mg/l in heterozygotes, 650-1000 mg/l in homozygotes

•

en:diverse tissue cell types (vascular endothelial cells, adipocytes, schwann cells, leukocytes) have membrane-lined cytoplasmic vacuoles with amorphous and filamentous material

•

en:defective t-cell proliferative responses (in some patients)

•

en:decreased reversible oxygen-binding capacity (e.g. hb l (bombay) 141800.9999)

•

en:decreased or absent peroxisome acyl-coa oxidase activity and protein

•

en:decreased high molecular weight plasma factor viii/ vwf multimers

•

en:glucose-6-phosphate deficiency

•

en:decreased amount and activity of mitochondrial complexes i and iv

•

en:decreased or low-normal serum parathyroid hormone (pth)

•

en:abnormal isoelectric focusing of serum transferrin (type 1 pattern) (in 1 patient)

•

en:elevated serum n,n-dimethylglycine (dmg)

•

en:abnormal urinary mucopolysaccharides (elevated unsaturated nonsulfated disaccharides and decreased unsaturated 6-sulfated disaccharides)

•

en:elevated 17-hydroxyprogesterone

•

en:decreased activity of glycosylceramidase, galactosylceramidase, ceramidase, and other lysosomal enzymes

•

en:abnormally triglyceride-rich low and high density lipoproteins and beta-migrating very low density lipoproteins

•

en:hyponatremic dehydration, rarely

•

en:absent platelet agglutination in presence of ristocetin

•

en:deficiency of saposins a, b, c, and d

•

en:elevated androstenedione and testosterone

•

en:argininosuccinic aciduria

•

en:urocanase deficiency

•

en:glycogen storage disease type v

•

en:abnormal serum transferrin pattern (in some patients)

•

en:branched chain ketoaciduria (alpha-keto isocaproate, alpha-keto-beta methylisovalerate, alpha-keto isovalerate)

•

en:characteristic spheroids can be found in peripheral tissue, such as skin and conjunctiva

•

en:decreased n-acetylglucosamine-1-phosphotransferase (glcnac - phosphotransferase) using lysosomal enzymes

•

en:decreased circulating cortisol level

•

en:defective bile acid metabolism

•

en:elevated leukotriene e(4)

•

en:elevated hepatic transaminases

•

en:3-methylglutaric aciduria (3-mga)

•

en:decreased serum glucosyltransferase (ggt) activity

•

en:exercise-induced myoglobinuria

•

en:abnormal liver enzymes, intermittent

•

en:galactocerebroside beta-galactosidase deficiency in serum, leukocytes, and fibroblasts

•

en:homocysteinemia (in some patients)

•

en:iduronate sulfatase deficiency in fibroblasts, amniocytes and white blood cells

•

en:elevated gamma-glutamyltransferase

•

en:abnormal isoelectric focusing of serum transferrin (type 1 pattern)

•

en:absent dystrophin on muscle biopsy

•

en:blunted cortisol response to adrenocorticotropic hormone (acth)

•

en:elevated hcg or afp or both (embryonal carcinoma)

•

en:bromosulfophthalein test - secondary rise at 90 minutes

•

en:decreased sulfite oxidase activity in fibroblasts

•

en:cytogenetic deletion of chromosome 19q13

•

•

en:hla-dqw6 association (dqb1*0602)

•

en:decreased activity of mitochondrial respiratory complexes i, ii+iii, iv, and v

•

en:factor viii deficiency

•

en:heparan sulfate excretion in urine

•

en:elevated serum bile acids

•

en:lactic acidemia (2p21del)

•

en:inappropriately normal to low-normal serum 1,25-dihydroxyvitamin d3

•

en:increased oxygen affinity (e.g. hb nunobiki 141800.0109)

•

en:increased platelet aggregation with ristocetin

•

en:increased serum iduronate sulfatase (10-20x)

•

en:increased serum c26-bile-acid intermediates

•

en:low pyruvate carboxylase activity in liver and cultured fibroblasts

•

en:increased urinary 2-hydroxybutyrate

•

en:increased urinary orotic acid (in some patients)

•

en:increased urinary, plasma, and csf n-carbamyl-beta-alanine

•

en:increased urinary acetoacetic acid

•

en:increased urinary, plasma, and csf d-2-hydroxyglutaric acid

•

en:low serum alkaline phosphatase in heterozygotes

•

en:low or absent prolactin (pl)

•

en:increased plasma renin activity

•

en:increased urinary tricarboxylic acid intermediates

•

en:androgens increased

•

en:platelet aggregation decreased

•

abêtalipoprotéinémie

•

en:holocarboxylase synthetase deficiency

•

en:elevated alkaline phosphatase

•

mucolipidose type ii

•

acidurie dicarboxylique

•

•

en:factor vii deficiency

•

hypofibrinogénémie

•

agrégation des plaquettes diminuée

•

maladie de tay-sachs

•

en:increased creatinine

•

en:decreased mitochondrial complex iii activity (in liver, muscle, and fibroblasts)

•

en:increased plasma 2-methylbutyrylcarnitine

•

en:low or absent adrenocorticotropic hormone (acth) in some patients

•

en:increased urinary cross-linked n-telopetide of type i collagen

•

en:electron microscopy of patient respiratory cells shows absent outer dynein arms

•

en:increased serum c4 and c5 acylcarnitine esters

•

en:decreased or normal serum factor i

•

en:deficient ribose-s-phosphate isomerase (rpi) in fibroblasts

•

en:high urinary orotic acid

•

en:elevated uric acid on urinalysis (in some patients)

•

en:igg, elevated

•

en:decreased-absent intestinal mucosa lactase activity

•

en:deficient hepatic 4-hydroxyphenylpyruvate dioxygenase

•

en:ferritin decreased

•

en:decreased or increased serum testosterone

•

en:decreased transcobalamin i in saliva, serum, gastric juice, and cerebrospinal fluid

•

en:hyperhomocystinemia

•

en:elevated propionate

•

en:elevated white blood cell cystine

•

en:hypocalcemia (male)

•

en:increased urinary oxylate

•

en:increased urinary excretion of camp

•

en:dicarboxylic aciduria

•

en:increased igg level

•

en:little to absent aspartylglucosaminuria activity

•

en:increased serum pancreatic secretory trypsin inhibitor (psti)

•

en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies) can be found in various tissues (brain, liver, muscle, heart, skin)

•

en:increased urinary 3-methylglutaconic acid

•

en:increased serum creatine kinase in acute stage

•

en:increased serum acylcarnitine during febrile crisis

•

en:increased cholesterol

•

en:methemoglobinemia

•

en:fatty alcohol:nad+ oxidoreductase deficiency in leukocytes and fibroblasts

•

en:decreased plasma esterified cholesterol

•

en:lack of ciliary motility

•

en:abnormal columnization of chondrocytes

•

en:abnormal liver enzymes in those with hepatic cysts or fibrosis

•

en:decreased erythrocyte 2,3-diphosphoglycerate (2,3-dpg)

•

en:cytosolic phosphoenolpyruvate carboxykinase deficiency

•

en:decreased levels of plasma vwf antigen

•

en:accumulation of sulfatides, glycosaminoglycans, sphingolipids, and steroid sulfates in tissues and body fluids

•

en:decreased serum acth

•

en:decreased activity of ampd1 in skeletal muscle increased serum creatine kinase

•

en:elevated serum transaminase levels

•

en:absence of hepatic udp-glucuronyl-transferase

•

en:bicarbonaturia

•

en:cytogenetic breakpoints range from 10q23.3-q26.2

•

en:balanced translocation carrier 46,xy,+(11:18)(p13:q21)mat

•

en:cytochrome c oxidase deficiency in skeletal muscle and brain

•

en:iiga and igg antigliadin antibodies (aga)

•

en:absence of cd59 expression on red cells

•

en:chylomicronemia, refractory fasting

•

en:elevated plasma luteinizing hormone (lh)

•

en:deficiency or absence of p47-phox protein (type i)

•

en:delta-1-pyrroline-5-carboxylate dehydrogenase activity decreased in fibroblasts or leukocytes

•

en:elevated serum alpha-fetoprotein

•

en:appropriately increased serum 1,25-dihydroxyvitamin d3

•

en:fumarase activity (mitochondrial and cytosolic) is decreased

•

en:elevated urine ceramide levels

•

en:elevated urinary delta-aminolevulinic acid and porphyrins

•

en:decreased tetrasialo-transferrin

•

en:decreased serum cholesterol (in some)

•

en:decreased plasma apolipoprotein c-ii

•

en:elevated long-chain acylcarnitine species (in some patients)

•

en:deficiency of mitochondrial isovaleryl-coa dehydrogenase in fibroblasts

•

en:decreased mitochondrial complex iii activity seen in muscle

•

en:decreased circulating renin level

•

en:electrolyte disturbances from intractable diarrhea

•

en:decreased alpha-n-acetylgalactosaminidase activity (less than 2% of control)

•

en:decreased activity of nadph oxidase

•

en:frequent deletions of chromosome 9 in melanoma

•

en:accumulation of guanidinoacetate in brain

•

en:elevated biopterin in csf

•

en:decreased serum l-transferrin (heterozygous patient)

•

en:elevated 2-ketoglutarate (urine)

•

en:decreased activity of succinic semialdehyde dehydrogenase (ssadh, aldh5a1), less than 5% of control values

•

en:elevated 3-methylcitric acid

•

en:broad tissue deposition of amylopectin-like material

•

en:decreased palmitate oxidation

•

en:defect in oxidative phosphorylation

•

en:decreased cerebrospinal fluid folic acid

•

en:elevated serum uric acid concentrations

•

en:decreased 3-beta-hydroxysteroid-delta-5-desaturase (sc5d)

•

en:amorphous hyaline substance (skin biopsy and visceral organs)

•

en:granular osmiophilic deposits (grod) in cells resulting in 'curvilinear' profiles ultrastructurally

•

en:absent ch50 activity in complete c4 deficiency

•

en:bilirubin conjugated increased

•

en:agammaglobulinemia

•

en:tay-sachs disease

•

en:decreased udp-glcnac

•

en:decreased serum igm

•

en:elevated urinary 3-methylglutarate

•

en:hyperkalemia

•

en:fasting hypoglycemia (early in disease course)

•

en:elevated alkaline phosphatase of bone origin

•

en:fibroblasts have increased activity of serine palmitoyltransferase (spt, 605712)

•

en:elevated urinary n,n-dimethylglycine (dmg)

•

en:abnormal bone marrow karyotype, t(8,21)

•

en:hyperkalemia (6.4 +/- 0.7 mm)

•

en:decreased or normal plasma insulin

•

en:elevated plasma galactose (galactosemia)

•

en:decreased erythrocyte lactate clearance (transport), 40 to 50% of normal values

•

en:chromosome 11q23.3 deletion

•

en:decreased tetrasialotransferrin levels

•

en:elevated l-2-hydroxyglutaric acid (urine)

•

en:defective dna repair after ultraviolet radiation damage

•

en:direct coombs test negative

•

en:absence of emerin by immunohistochemistry on muscle biopsy

•

en:galactosuria

•

en:decreased short/branched-chain acyl-coa dehydrogenase protein levels and enzyme activity

•

en:decreased serum luteinizing hormone (lh)

•

en:decreased glomerular filtration rate (gfr)

•

en:low or absent thyroid-stimulating hormone (tsh)

•

en:low 25-oh-vitamin d level

•

en:increased tissue long-chain acylcarnitines

•

en:increased lactate in spinal fluid

•

en:increased urinary alpha-ketoglutaric acid, intermittent

•

en:low serum levels of ketone bodies

•

en:low-normal platelet count (89-290 x 10(9)/l)

•

en:increased erythrocyte-membrane calcium-magnesium-atpase

•

hypertriglycéridémie

•

en:low or undetectable c-peptide

•

en:lack of excessive parenchymal iron storage

•

en:isovalericaciduria

•

en:leukocyte inclusion bodies (em) - intermediate filaments and ribosome clusters irregularly dispersed in cytoplasm

•

en:increased urinary citric acid cycle intermediates

•

en:increased urinary o-linked sialopeptides

•

en:increased total bilirubin may occur

•

en:increased urinary thiosulfate

•

en:decreased activity of branched-chain ketoacid dehydrogenase (bckdh)

•

en:increased fibroblast free sialic acid

•

•

en:thrombopenia

•

en:hypernatraemia

•

en:defibrination syndrome

•

•

en:hyperlipoproteinemia type I

•

•

bicarbonate sérique augmenté

•

en:absent 7-dehydrocholesterol

•

en:increased urinary s-(2-carboxypropyl)cysteine

•

acidémie glutarique de type 1

•

hyperlipidémie

•

•

thrombocytopénie

•

•

cholestérol sanguin élevé

•

déficit en vitamine D

•

en:increased csf immunoglobulin levels

•

hyperphosphatémie

•

en:low plasma tryptophan (inflammatory type b)

•

en:impaired carnitine uptake in muscle, heart, kidney, fibroblasts, and lymphocytes

•

en:hla-b27 haplotype association (95% patients)

•

en:carnitine palmitoyltransferase ii deficiency (25% of controls)

•

en:decreased plasma glycine

•

en:abnormal extrarenal response to ddavp (no increase in von willebrand factor or factor viii)

•

en:elevated serum alpha-fetoprotein (dominant)

•

en:hepatic lipase deficiency (disorder)

•

en:beta-galactosidase deficiency in fibroblasts and white blood cells

•

en:fumarylacetoacetate hydrolase (fah) deficiency

•

en:impaired response to gm-csf

•

en:growth cartilage disorganized, with islands of cells and abnormal collagen arrangement

•

en:hyperglycinuria (disorder)

•

en:decreased plasminogen activity

•

en:elevated blood spot hydroxybutyryl carnitine

•

en:hyperchloremia (mean >110 mm in both dominant and recessive)

•

en:ketoses, metabolic

•

en:hyperammonemia, asymptomatic (2-5 times normal)

•

en:hypercholesterolemia (in 75%)

•

en:decreased heme-heme interaction (e.g. hb kanagawa 141800.0169)

•

en:increased lactate: pyruvate ratio (group b)

•

en:homocysteinemia

•

en:increased serum arylsulfatase a (10-20x)

•

en:increased hepatic parenchymal cell stainable iron

•

en:increased urinary 2-oxoglutaric acid

•

en:increased serum lactate in acute stage

•

en:increased long-chain acylcarnitine

•

en:increased csf threonine

•

en:anomalies of cholesterol levels

•

en:elevated inflammatory markers

•

en:hypoproteinemia due to hypercatabolism

•

en:decreased serum complement factor h

•

en:elevated testosterone

•

en:low level of c4 and c2

•

en:detection by rt-pcr, southern blot analysis, and fish for primary diagnosis and follow up for residual disease

•

en:electron microscopy of patient respiratory cells shows defects in inner and outer dynein arms

•

en:hepatic argininosuccinase deficiency

•

en:elevated plasma follicle stimulating hormone (fsh)

•

en:decreased conversion of beta-carotene to vitamin a (retinol)

•

en:absent anti-insulin receptor antibodies

•

en:decreased fibroblast beta-hexosaminidase

•

en:'rectilinear profiles' ultrastructurally in cells

•

en:abnormal myelination in sural nerve biopsies

•

en:deficiency or absence of p22-phox (608508) protein

•

en:hypouricemia

•

en:decreased gtp cyclohydrolase i activity (about 20% of normal)

•

en:decreased peroxisomal fatty acid beta-oxidation

•

en:decreased thrombospondin

•

en:defect in n- and o-glycosylation

•

en:decreased fibroblast alpha-mannosidase

•

en:high serum osmolality

•

en:axonemes show normal structure

•

en:decreased activity of ppt1

•

en:hepatic argininosuccinate synthetase deficiency

•

en:glyoxalase deficiency

•

en:elevated serum phosphorus

•

en:decreased natural killer cells

•

en:alpha ketoadipic aciduria

•

sérum

•

en:heteroplasmic partial duplication of mtdna

•

en:elevated 7-dehydrocholesterol

•

en:hypertriglyceridemia (rare)

•

en:elevated serum transferrin saturation

•

en:abnormal phospholipid profile

•

en:abnormal glycosylation of serum transferrin, type 1 pattern

•

en:abnormal response to human chorionic gonadotropin indicates decreased testosterone

•

en:elevated sed rate

•

en:elevated serum protein

•

en:decreased csf 5-hydroxyindoleacetic acid (5-hiaa)

•

•

en:propionic acidemia

•

en:blood urea nitrogen increased

•

en:indirect hyperbilirubinemia

•

en:absent alkyl-dhap synthase activity

•

en:decreased activities of multiple sulfatases

•

en:4-hydroxyphenylpyruvic acid dioxygenase deficiency (hpd)

•

en:decreased complement factor d

•

en:elevated erythrocyte aicar (zmp)

•

en:dermatan sulfate excretion in urine

•

en:elevated serum parathyroid hormone (pth)

•

en:elevated csf/plasma glycine ratio

•

en:b lymphocytopenia

•

en:hyperglycemias, postprandial

•

en:elevated il1-beta

•

en:depletion of mtdna (skeletal muscle, fibroblasts)

•

en:hypomethylation of alpha-satellite repeats on chromosome 9

•

en:decreased methionine synthase activity

•

en:4-hydroxyphenylacetic aciduria

•

en:elevated fecal levels of protoporphyrin and coproporphyrin at all times

•

en:disturbed visual and brainstem auditory evoked responses indicative of cns demyelination

•

en:hyperglycolic aciduria

•

en:abnormal spinocerebellar tracts, dorsal columns, pyramidal tracts, cerebellum and brainstem

•

en:guanidinoacetate methyltransferase (gamt) deficiency

•

en:4-hydroxyphenylpyruvic aciduria

•

en:elevated plasma methionine (methioninemia)

•

en:hyperglutaminemia

•

en:elevated progesterone

•

en:erythrocyte delta-aminolevulinate dehydratase (alad) deficiency

•

en:increased n-acetyl-l-aspartic acid (naa) in urine, csf, and blood

•

en:elevated erythrocyte adenosine deaminase

•

en:isovalerylglycinuria

•

en:increased urinary prostaglandin e2

•

en:intracellular fingerprint profiles on ultrastructural analysis

•

en:low levels of serum mg(2+) in the absence of other electrolyte disturbances

•

en:increased serum lactate

•

en:large spermatozoa

•

en:loss of heterozygosity in giant cell astrocytomas, angiomyolipomas, rhabdomyomas

•

en:increased csf transferrin despite normal serum transferrin levels

•

en:low maximal oxygen uptake on exercise testing

•

en:increased urinary dopamine

•

en:increased serum lysine (group b)

•

en:increased urinary neopterin

•

en:intracellular redox disturbance (reduced cytoplasm and oxidized mitochondria (group b))

•

en:increased urinary formiminoglutamic acid (figlu)

•

en:increased serum levels of free plasma thyroid hormones

•

carence en vitamine D

•

en:serum cholesterol raised

•

en:thrombocytopenia

•

a-bêta-lipoprotéinémie

•

hypo-bêta-lipoprotéinémie

•

en:'ghost' peroxisomes in fibroblasts seen on immunofluorescence microscopy

•

carence en vitamine d

•

en:hypophosphatasia infantile

•

hématurie microscopique

•

en:hereditary factor x deficiency

•

abêtalipoprotéinémie normotriglycéridémique de type Steinberg

•

•

en:dilated rough endoplasmic reticulum (rer)

•

en:increased serum creatine kinase during episodes

•

en:increased urinary catecholamines

•

en:increased serum glutamine

•

en:increased 11-deoxycortisol

•

en:hypobetalipoproteinemias

•

en:increased acetylcholinesterase (ache) in amniotic fluid

•

en:elevated serum lactate

•

en:hypocalcemia, transient

•

en:glucosuria, mild, intermittent

•

en:elevated crp

•

en:immotile or weakly motile cilia

•

en:elevated erythrocyte sedimentation rate (esr)

•

en:hypertriglyceridemia, transient

•

en:decreased fibrillin-1 immunostaining in the dermis

•

en:decreased plasma total and free carnitine

•

en:increased 18-ohb to aldosterone ratio

•

en:increased interleukin 10

•

en:iga antiendomysial antibodies (ema)

•

en:increased serum butyryl carnitine

•

en:increased urinary thymine

•

en:increased serum methionine (reported in 2 cases)

•

en:increased urinary hydroxyisovaleric acid

•

en:increased urinary levels of maoa substrates (endogenous bioamines)

•

en:incresased urinary pyruvate

•

en:intracellular accumulation of unesterified cholesterol

•

en:increased urinary 2-methyl-3 hydroxybutyrate

•

en:increased serum s-adenosylhomocysteine

•

en:increased interferon-alpha signal

•

en:increased serum transaminases (in 1 of 3 patients)

•

en:increased c10:2-carnitine

•

en:increased vitamin e (alpha-tocopherol) levels

•

en:increased blood alanine

•

en:decreased or absent alpha-n-acetylgalactosaminidase activity

•

hydrocortisone diminuée

•

en:hypertriglyceridemia

•

en:diaminoaciduria (arginuria, lysinuria, cystinuria, ornithinuria)

•

en:decreased serum haptoglobin

•

en:decreased beta-mannosidase activity in plasma, fibroblasts, and leukocytes

•

en:homozygous 122kb deletion 11p15-p14

•

en:decreased activity of 2-oxoacid dehydrogenases

•

en:decreased or absent glycogen branching enzyme activity

•

en:decreased fumarate hydratase activity

•

en:csf pleocytosis, particularly of lymphocytes

•

en:decreased lysosomal alpha-mannosidase activity in plasma and leukocytes

•

en:hematuria (less common)

•

en:absent or severely reduced levels of serum immunoglobulins

•

en:decreased copper, iron, zinc

•

en:aminoadipic semialdehyde synthase (aass) deficiency

•

en:diminished lymphocyte response to phytohemaglutinin

•

en:allelic loss on 16p13.3 in angiomyolipoma, cardiac rhabdomyoma, cortical tuber, and giant cell astrocytoma

•

en:decreased carnitine palmitoyltransferase ii (cpt2) activity

•

en:decreased urinary calcium and phosphate excretion

•

en:elevated gamma-glutamyltransferase (ggt)

•

en:abnormal isoelectric focusing of serum transferrin (type 1 pattern without increase of asialotransferrin)

•

en:decreased activity of mitochondrial respiratory chain complex i

•

en:elevated alpha-ketoglutarate (in most patients)

•

en:decreased scad activity

•

en:deficiency of laminin alpha-2 chain of merosin (lama2, 156225) in muscle

•

en:decreased csf 5-hydroxyindoleacetic acid (5hiaa)

•

en:decreased activity of 3-methylcrotonyl-coa carboxylase (less than 2%)

•

en:abnormal oral glucose tolerance

•

en:elevated d-2-hydroxyglutaric acid (urine, plasma, csf)

•

en:bilirubin may or may not be increased

•

en:decreased levels of cpt2 protein

•

en:duplication or deletion at 11p15.5

•

en:giant cells (degenerating chondrocytes) in resting zone of epiphyseal cartilage

•

en:calcium normal

•

en:absence of cpt ii protein

•

en:anti-tissue transglutaminase antibodies (anti-ttg)

•

en:decreased cpt1 activity

•

en:decreased plasma and urinary guanidinoacetate (gaa)

•

en:antiribonuclear protein positive

•

en:cytogenetic deletion of the terminal region of chromosome 10 (del(10)(q23.3-qter))

•

en:cytogenetics - recombinant chromosome 8 characterized by duplication of 8q22.1-qter and deletion of 8pter-p23.1

•

en:abnormal igfr1 function

•

en:acetyl coa:alpha-glucosaminidase n-acetyltransferase deficiency in fibroblasts

•

en:decreased prpp synthetase activity in erythrocytes and fibroblasts

•

en:aminoaciduria, mild (in some patients)

•

en:elevated urinary 2-ethylhydracrylate

•

en:absence of chylomicrons in lymph and plasma

•

en:platelet function test normal

•

en:decreased beta-thromboglobulin

•

en:liver enzymes abnormal

•

en:thyroid dyshormonogenesis 4

•

en:acyl-coa:dihydroxyacetonephosphate acyltransferase deficiency

•

en:elevated apoa-i (1.8x normal) in homozygotes

•

en:abnormal liver enzymes (1 patient)

•

en:decreased activity of 3-hydroxyacyl-coa dehydrogenase in various tissues (liver, muscle, fibroblasts)

•

en:hyperchloridura

•

•

en:decreased plasma total cholesterol

•

en:decreased transferrin increased serum iron

•

en:decreased galactokinase activity

•

en:hyperthreoninemia

•

en:hypoglycosylated serum transferrin

•

en:elevated cholesta-8,14-dien-3-beta-ol in cultured fibroblasts

•

en:electron microscopy of patient respiratory cells shows reduced inner dynein arms and nexin links

•

en:hemizygous deletion at 7q11.23

•

en:elevated serum glutamic oxaloacetic transaminase (sgot)

•

en:erythrocyte porphobilinogen (pbg) deaminase deficiency (exception: type ii aip)

•

en:dolichyl-p-glc:man(9)glcnac(2)-pp-dolichyl glucosyltransferase deficiency

•

en:decreased hexokinase activity in red blood cells

•

en:elevated il6

•

en:decreased expression of gpi-anchored proteins on blood cells

•

en:hyperammonemia after protein intake

•

en:decreased csf serine

•

en:increased serum osteocalcin

•

en:marked elevation of serum c-reactive protein level (crp 123260)

•

en:increased lysine in serum and csf

•

en:increased urinary hypoxanthine

•

en:increased plasma and urinary pipecolic acid

•

en:increased growth hormone (in 1 of 2 patients)

•

en:increased igm level

•

en:increased cerebrospinal fluid (csf) protein (>100mg/dl)

•

en:low or normal serum calcium

•

en:increased chromosomal rearrangements (bone marrow and fibroblast culture)

•

en:increased serum acylcarnitines

•

en:increased 18-hydroxycortisol

•

en:increased serum, urinary, and csf lysine

•

en:decreased or absent serum and urinary chenodeoxycholic acid and cholic acid

•

en:lactate high

•

en:low or normal serum erythropoietin

•

en:increased urinary carnitine esters

•

en:iron overload (in some patients)

•

•

cétose de jeûne

•

en:Bassen-Kornzweig's disease

•

en:transferase deficiency galactosemia

•

•

coagulation intravasculaire disséminée

•

•

en:secondarily decreased activity of the pyruvate dehydrogenase complex (pdc)

•

en:ketoacidosis

•

en:hyperammonemia during episodes

•

en:intermediate level of cellular sensitivity to uv light

•

en:increased urinary 2-methylbutyryl glycine

•

en:increased urinary potassium

•

en:increased serum triiodothyronine (t3)

•

en:low urinary orotic acid

•

en:increased serum acyl carnitines

•

en:irregular distribution of chondrocytes, enlarged chondrocyte lacunae, excessive fibrous matrix, perilacunar loss of glycosaminoglycan, excessive collagen aggregation

•

en:increased serum, cerebrospinal fluid, and urinary levels of alpha-aminoadipic semialdehyde

•

en:increased urinary organic acids (in some patients)

•

en:chronic hypoxemia

•

en:increased erythrocyte sedimentation rate, episodic

•

en:fibroblasts show decreased activity of mitochondrial respiratory complex i, complex iii, complex iv, and complex v

•

en:decreased dihydroxyacetone phosphate acyltransferase (dhap-at) activity

•

en:high newborn serum levels of immunoreactive trypsinogen

•

en:hypoalbuminemia (in 83%)

•

en:fibroblasts show hypersensitivity to uv irradiation due to defect in transcription-coupled nucleotide excision repair (tc-ner)

•

en:decreased csf 3-methoxy-4-hydroxyphenylethyleneglycol (mhpg)

•

en:delayed plasma clearance of unconjugated bromsulphthalein, an anionic diagnostic dye

•

en:decreased plasma triglycerides

•

en:deficiency or absence of p91-phox protein

•

en:glucosidase i deficiency in liver and fibroblasts

•

en:decreased plasma hdl (<1/10 of normal levels)

•

en:elevated 3-hydroxypropionic acid

•

en:elevated plasma ornithine (~10-fold)

•

en:decreased plasma and urinary ornithine

•

en:characteristic urinary coproporphyrin pattern (mostly isomer i (80%) instead of isomer iii)

•

en:chromosome instability (hypo-/hyperdiploidy, chromosomal breaks, premature centromere division)

•

en:cytoplasmic lamellar concentric inclusions

•

en:increased chromosomal breaks in response to cross-linking agents and ionizing radiation

•

en:increased sensitivity to adrenergic and cholinergic agents

•

en:increased activity of the prpp synthetase 1 enzyme

•

en:premature separation of centromeric heterochromatin

•

en:glucose breath hydrogen test shows malabsorption of glucose and galactose

•

en:amyloidosis, (iowa type 107680.0010, nonneuropathic 107680.0016)

•

en:immunoglobulin a decreased

•

en:generalized amyloid deposition

•

en:elevated pth (parathyroid hormone)

•

en:deficiency of alpha-1,4-glucosidase (acid maltase)

•

en:hyperthreoninuria

•

en:elevated serum levels of adenosine

•

en:gamma-glutamylcysteine synthetase (glutamate-cysteine ligase) deficiency

•

en:hypokalemia occurs during paralytic attacks

•

en:igm deficiency

•

en:Leroy's i-cell disease

•

hématurie macroscopique

•

en:glutaric aciduria, type 1

•

en:hyperlipoproteinemia type iib

•

mucolipidose type II

•

en:defective DNA repair

•

•

en:abnormal isoelectric focusing of serum transferrin, type 2 pattern

◀

• Mathieu Lafourcade • LIRMM (données libres en Creative Commons - C0 domaine public) •

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=6880835 • caches: c1=8 c2=1002 c3=1

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