Diko : en:muscle weakness of limb

en:muscle weakness of limb

Catégories

Nom

Informations lexicales

Langue:anglais

Liens externes

›

umls:C0587246

Inhib

⊗

›

fièvre

(surexcitation)

•

fièvre

(trouble de l'âme)

•

épiphyse

(os)

Associations d'idées

[F]

›

1000

parésie des membres

•

en:distal muscle atrophy, predominantly lower limbs

•

en:increased numbers of abnormally-shaped mitochondria in subsarcolemmal areas

•

en:muscle weakness (in 90% of patients)

•

en:muscle biopsy shows dystrophic features

•

en:atrophy of the thenar and hypothenar muscles

•

en:fiber type variation seen on biopsy

•

en:muscle biopsy shows no dystrophic changes

•

en:fibrillations in affected muscles

•

en:mitochondrial proliferation

•

en:attacks precipitated by cold temperature

•

en:hamstring muscle affected

•

en:decreased muscle mass (predominantly in lower extremities)

•

en:atrophic muscle fibers

•

en:fiber necrosis

•

en:prominent veins, lower limbs

•

en:fatty deposition

•

en:hangrip myotonia

•

en:atrophic calf muscles

•

en:angulated atrophic muscle fibers

•

en:cellulitis or infection may occur

•

en:decreased immunostaining for alpha-sarcoglycan

•

en:decreased mitochondria

•

en:acetazolamide may worsen symptoms

•

en:increased lysosomal glycogen

•

en:absence of myotonia in infancy (congenital form)

•

en:abnormal irregular myofibrillar network

•

douleur de la face

•

en:muscle cramps, painful, recurrent

•

en:muscle biopsy shows glycogen accumulation in myofibrils and lysosomes

•

fibrillation

•

en:subsarcolemmal accumulations of abnormally shaped mitochondria seen on electron microscopy

•

en:tendon tears

•

en:distal limb muscle weakness (less common)

•

en:normal or increased adipose tissue around the neck

•

en:redundancy of basal lamina with accumulated debris

•

en:subsarcolemmal lipofuscin-positive deposits

•

en:increased connective tissue

•

en:dense membranous structure surrounding nuclei on electron microscopy

•

en:upper limb weakness

•

en:cores contain densely packed myofilaments

•

en:lower limb muscle atrophy (in 2 of 3 families)

•

en:abnormal muscle fibers with amorphous, granular, or hyaline deposits

•

en:abnormal glycosylation of alpha-dystroglycan seen on muscle biopsy

•

en:vacuoles are autophagocytic and contain granular and membranous cellular debris

•

en:proximal muscle weakness (85% of patients)

•

en:nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic)

•

en:muscle pain (less common)

•

en:muscular dystrophy with variable age of onset (infancy to young adult)

•

en:peroneal muscle atrophy

•

en:lipomas or lipomatous masses (most cases)

•

en:muscle wasting (especially legs and arms)

•

en:muscle fiber atrophy, profound (rare)

•

en:proximal muscle weakness more severe than distal muscle weakness

•

en:patients may have distal or proximal muscle weakness, or both

•

en:no muscle fiber necrosis

•

en:muscle biopsy shows lipid droplets

•

en:muscle biopsy shows myofibrillar disruption

•

en:myopathy (rare)

•

leuco-encéphalopathie

•

en:dizziness

•

en:type 1 muscle fiber predominance

•

perte de connaissance

•

en:dystonia

•

en:refsum disease

•

en:infantile nystagmus

•

en:interictal downbeat nystagmus

•

en:abnormal visual evoked potential (vep)

•

en:abnormal subcutaneous fat tissue distribution

•

en:psychomotor agitation

•

en:agnosia

•

en:cerebral hemorrhage

•

en:mitochondrial myopathy

•

en:leg cramp

•

en:myasthenias

•

en:atrophy

•

en:asthenia legs

•

neuralgie trigéminale

•

en:meningioma

•

en:seizure disorder

•

en:predominantly lower limb lymphedema

•

en:cerebral cavernous malformation

•

en:dural ectasia

•

en:pyramidal type muscle weakness

•

en:different temperature in opposite limbs

•

en:vertigo

•

migraine avec aura

•

paraplégie spastique

•

rétinite pigmentaire et retard mental

•

en:dyskinesia

•

en:encephalocele of orbit

•

maladie cérébrovasculaire aiguë mal définie

•

en:atrophy of the lower leg muscles

•

AVC

•

accident cérébro-vasculaire

•

démence fronto-temporale

•

en:high pain threshold

•

en:eighth cervical nerve

•

en:focal loss of cross striations seen on muscle biopsy

•

en:reduced muscle tone

•

en:decreased numbers of acetylcholine receptors (achr) in the postsynaptic membrane (less than 50% of normal)

•

en:lipid storage, mainly in type i fibers

•

en:repetitive action potentials in response to single nerve stimulation

•

en:nerve conduction velocities normal or near-normal

•

en:abnormal fiber size variation

•

schizophrénie

•

en:spongy degeneration

•

en:diffuse slow background activity seen on eeg

•

en:spike-wave discharges

•

syncope psychogène

•

en:blackout - symptom

•

en:olivopontocerebellar hypoplasia, fetal-onset

•

en:nystagmus, horizontal

•

en:head titubations

•

en:head oscillations

•

en:frontolimbic dementia

•

en:demyelinating polyneuropathy

•

en:aura

•

en:loss of proprioception

•

en:eye muscle weakness

•

en:decreased activities of mitochondrial-encoded respiratory chain complexes

•

paralysis

•

en:adipose tissue shows many adipocytes with multiple small lipid droplets rather than a normal single lipid droplet

•

dystonie

•

en:power failure

•

en:white material

•

en:piss with rain

•

prendre une bûche

•

en:heredo-ataxia hemeralopica polyneuritiformis

•

en:pour with rain

•

se casser la margoulette

•

lymphangiectasie

•

en:muscular weakness

•

torticolis

•

en:infarct

•

en:general paresis

•

en:rotary vertigo

•

en:facial edema

•

en:progressive cerebellar degeneration

•

en:balance problem

•

en:to fall

•

en:epileptiform neuralgia

•

bosse de bison

•

agnosie

•

cordon nerveux

•

trouble de l'équilibre

•

en:cataplexis

•

stroke

•

en:stroke

•

douleur faciale

•

en:cardiac arrest

•

syncope bleue

•

en:motor disability

•

incontinence paradoxale

•

en:hypotonia, neonatal and later

•

Trouble mental

•

en:with growth retardation

•

en:ophthalmoplegia

•

déficience mentale

•

en:defective speech

•

en:to debase o.s.

•

en:power shutdown

•

en:fervescence

•

en:rain pitchforks

•

s'étaler de tout son long

•

altération de la conscience

•

Malformation d'Arnold-Chiari

•

Refsum (maladie de)

•

Voile noir

•

en:come pelting down

•

en:descend upon somebody

•

en:delayed myelination endocrine : gonadotropin-dependent precocious puberty (1 patient)

•

en:dorsal nerve cord

•

pleuvoir à seaux

•

en:illicitly

•

en:asphyxia

•

démence héréditaire et infarctus multiples cérébraux

•

Gayet-Wernicke-Korsakoff (encéphalopathie de)

•

méningo-encéphalite

•

en:paralytic dementia

•

paraplégie spastique familiale

•

autophagosome

•

en:epilepsia partialis continua

•

en:sensorimotor axonal and demyelinating polyneuropathy

•

en:pectoralis major hypoplasia

•

en:fasciculations (less common)

•

en:muscle weakness, severe

•

en:muscle weakness, proximal, distal, and axial, severe

•

en:cores with lack of oxidative activity and mitochondrial depletion may also be found and extend along length of fiber

•

en:skeletal muscle shows decreased sarcoglycan proteins

•

en:nonspecific myopathic changes seen on biopsy

•

en:absence of gamma-sarcoglycan protein

•

en:respiratory distress (congenital form)

•

en:muscle weakness due to peripheral neuropathy

•

en:muscle biopsy shows decreased or absent dysferlin staining

•

en:onset of lymphedema around puberty

•

en:exertional leg pain

•

en:lipid droplets seen on muscle biopsy

•

en:loss of lower-limb tendon reflexes

•

en:neurogenic atrophy seen on muscle biopsy

•

en:dystrophic features and atrophic fibers seen on muscle biopsy

•

en:myopathy, mild to severe

•

en:muscle fibers are immunoreactive for desmin and vimentin

•

en:amyloid deposition in muscle fibers occurs rarely

•

en:atrophy of type 1 and type 2 fibers

•

en:pelvic muscle involvement occurs later

•

en:muscle hyperirritability

•

en:hamstring and quadriceps muscles mildly affected

•

en:imaging shows muscle atrophy and fatty replacement

•

en:autophagic vacuoles seen on biopsy (in some patients)

•

en:disorganization of the myofibrillar pattern

•

en:glycogen accumulation seen on biopsy

•

en:skeletal muscle damage

•

en:decreased hand grip strength

•

en:scapular muscle atrophy

•

en:angulated fibers

•

atrophie musculaire neurogénique

•

nerf cardio-pneumo-entérique

•

démence

•

épiphyse

(glande pinéale)

•

en:hypogeusia

•

en:ubiquinone decreased

•

altération mentale

•

en:glial cell

•

en:stroke (rare)

•

en:mallory-like bodies

•

en:necrotic fibers

•

en:vacuolar membranes immunostain with sarcolemmal proteins

•

?il

•

en:some subcutaneous adipose tissue may remain on upper arms

•

en:muscle biopsy shows increased subsarcolemmal vacuolar glycogen accumulation

•

en:neck and proximal limb muscle myopathy

•

en:cranial muscles spared

•

en:subsarcolemmal hyaline bodies in type 1 fibers only

•

en:minicores or core-like regions may be present

•

en:increased adipose fibrosis

•

en:upper limb involvement occurs later or not at all

•

en:rimmed vacuoles with basophilic granular material

•

en:muscle weakness, predominantly proximal (in some patients)

•

en:rectus medial atrophy

•

en:swelling of the hands and feet (in 1 patient)

•

en:calf hypertrophy (early in the disease)

•

en:multiple mitochondrial respiratory enzymes deficiencies seen on biopsy

•

en:involves upper and lower proximal muscles

•

en:decreased muscle mitochondrial aconitase

•

en:lipohypoplasia, regional

•

en:biopsy shows myopathic and dystrophic changes

•

en:myopathy, nonprogressive

•

en:difficulty walking on heels occurs prior to difficulty walking on toes

•

en:episodic, nonerythematous, nonpruritic, nontender edema, episodic

•

en:marked lack of adipose tissue

•

en:limb-girdle muscle weakness (2 families)

•

en:muscle biopsy shows increased variation in fiber size

•

en:intrasarcoplasmic dense granulofilamentous aggregates that are immunoreactive with desmin

•

en:lymphoscintigraphy shows impaired lymphatic uptake and drainage

•

en:generalized muscular appearance from birth

•

en:muscle biopsy shows centralized nuclei

•

en:distal muscle weakness and atrophy

•

en:muscle biopsy shows small, membrane-bound vacuoles predominantly in type 2 fibers

•

en:muscle biopsy shows peripheral accumulation of abnormal mitochondria

•

en:muscle biopsy shows fiber type variation (in some patients)

•

en:impaired toe-walking

•

en:exertional fatigue

•

en:impaired heel-walking

•

en:disruption in the basal lamina seen on skeletal muscle biopsy

•

en:easy bruisability of lower extremities

•

en:distal limb muscle weakness and atrophy

•

en:decreased cytochrome c oxidase activity

•

en:distal lower limb amyotrophy

•

en:onset of weakness in hands and feet

•

en:increased central nucleation

•

en:secondary hypertrophy

•

en:muscle weakness, hypokalemia-related

•

en:normal or decreased facial and neck adipose tissue

•

en:centralized nuclei may be seen

•

en:increased fat and fibrous tissue

•

en:atrophic fibers

•

en:distal atrophy of the legs

•

en:calf hypertrophy (uncommon)

•

en:decrement of the compound muscle action potential on repetitive stimulation

•

en:swelling of the hands and feet, episodic

•

en:abnormal changes in the organization of the sarcolemma and the subsarcolemmal membrane cytoskeleton

•

en:both type 1 and type 2 fiber predominance has been reported

•

en:tremor of the upper limb

•

en:calf muscle hypertrophy

•

en:some patients never achieve ambulation

•

en:limb weakness and atrophy

•

en:myofibrillar disintegration

•

en:superior rectus atrophy

•

en:difficulty climbing stairs, jumping, running

•

en:proximal muscle weakness (occasional)

•

en:rhabdomyolysis may occur

•

en:retroperitoneal fibrosis (rare)

•

en:type 1 fiber atrophy seen on muscle biopsy

•

en:mild weakness

•

en:muscle fatigability

•

en:myopathic features seen on biopsy

•

en:nemaline bodies occur in type 1 fibers

•

en:hypotonia (2 patients)

•

en:muscle weakness following prolonged exercise

•

en:muscle atrophy (in some patients)

•

en:denuded postsynaptic regions

•

paraplégique

•

en:abdominal muscle hypoplasia

•

en:mental retardation

•

en:long perforating arteries of the brain are affected

•

en:myokymia

•

en:tremor

•

en:tremor of hands

•

en:pseudotumor cerebri

•

en:brain abscess

•

en:spinal arteriovenous malformation

•

encéphalite

•

oedème de la face

•

en:mobius syndrome

•

en:berardinelli-seip congenital lipodystrophy

•

en:cytochrome-c oxidase deficiency

•

en:peripheral neuropathy (smq)

•

faiblesse du muscle

•

en:psychiatric disorder

•

maladie de trousseau

•

en:paresis

•

en:dysautonomia

•

en:urinary incontinence

•

en:cauda equina syndrome

•

en:hemorrhage

•

en:drop attack

•

en:torticollis

•

en:isaacs syndrome

•

en:subjective muscle weakness

•

en:unilateral weakness of limbs

•

en:by fourth decade, many patients need help with ambulation

•

en:weakness of hand

•

en:cerebellar degeneration

•

en:attacks relieved by potassium administration

•

en:lafora bodies (accumulation of polyglucosan) seen on skeletal muscle biopsy

•

en:difficulty walking, running, climbing stairs

•

en:ascites (in some patients)

•

en:congophilic deposits

•

lipome

•

en:granulovacuolar degeneration

•

tremor

•

accident ischémique cérébral

•

en:hypothalamus

•

accident vasculaire cérébral

•

déficit en cytochrome oxydase

•

en:muscle weakness (hcs)

•

en:distal muscle weakness of the lower limbs secondary to peripheral neuropathy

•

en:hypotonia, generalized, severe

•

en:edema limbs

•

en:nystagmus, mild

•

en:lymphedema (primarily in lower limbs, but also arms in some patients)

•

en:myopathic features seen on emg

•

en:proximal muscle weakness, upper and lower limbs, due to peripheral neuropathy, later in disease course

•

en:distal muscle weakness due to peripheral neuropathy, lower limbs more affected than upper limbs

•

en:decreased numbers of postsynaptic nerve terminals at the neuromuscular junction

•

en:molar tooth sign seen on brain imaging

•

en:axial hypertonia

•

en:dyscalculia

•

asthénie neuro-circulatoire

•

encéphalopathie porto-cave

•

coma hépatique

•

en:congenital cerebellar hypoplasia

•

en:dysmyelinating leukodystrophy

•

en:dependent edema after excess fat has been present for several years

•

polio

•

en:decreased lactate clearance from muscle after exercise (reported in 1 patient)

•

en:disorder of equilibrium

•

déficience intellectuelle

•

pneumogastrique vagus

•

en:fail at a business

•

en:eat shit

•

prendre un gadin

•

en:fall into ruins

•

demi-saison

•

en:pour down with rain

•

en:fall to the floor

•

en:go down for the count

•

en:brains

•

en:fall down

•

en:disturbance of consciousness

•

en:effort syndrome

•

en:cranial nerve palsy

•

empâtement de la nuque et du cou

•

poussée fébrile

•

faire une chute

•

spasme carpopédal

•

en:generalized weakness of limb muscles

•

blindness

•

en:hyporeflexia (family a)

•

en:plantar fibromatosis

•

en:opisthotonus (patient b)

•

en:mild endplate myopathy

•

atrophie musculaire neurogène

•

en:set of astrocytes

•

en:oedema

•

en:atypical absence seizure

•

abcès du cerveau

•

en:mental dullness

•

rabaisser quelque chose

•

en:ophthalmic headache

•

en:and proeminent incisors

•

dégénérescence vacuolaire

•

en:low maximum workload on exercise testing

•

en:trachelocyllosis

•

en:demean o.s.

•

en:chuck down

•

se dégrader

•

en:motor handicap

•

en:to have a breakdown

•

en:oligergasia

•

en:belt down

•

retard mental, retard de croissance, surdité, microgénitalisme lié au sexe

•

multiracial

•

hémorragie intracrânienne

•

surdi-mutité

•

maladie de Gélineau

•

en:distal upper limb amyotrophy

•

Système nerveux autonome

•

en:ventral nerve cord

•

tomber à seaux

•

débilité mentale

•

en:tenth cerebral nerve

•

hypokinésie

•

en:neonatal distress

•

en:biopsy peripheral nerve normal

•

nerf sympathique

•

en:rhaebocrania

•

en:hydrocephalus

•

en:muscle fiber splitting

•

en:retain some mechanical adipose tissue (joints, orbits, palms, soles)

•

en:head drop due to neck muscle weakness

•

en:muscle weakness, proximal, pelvic girdle (in severe cases)

•

en:rhabdomyolysis with exercise (in older patients)

•

en:muscle pain and cramps following exercise

•

en:secondary myopathic changes

•

en:muscle biopsy in acute stage shows increased numbers of abnormal mitochondria

•

en:reduced ankle dorsiflexion

•

en:muscle weakness, limb-girdle, mild

•

en:myoclonic spasms

•

en:dorsal and flexor muscles of the forearm are involved

•

en:myofibrillar disorganization

•

en:difficulty running or inability to run

•

en:muscle biopsy shows decreased muscle-specific phosphorylase kinase activity

•

en:lower limb muscle hypotrophy

•

en:muscle weakness, lower limbs, during exercise

•

en:type 1 and type 2 muscle fibers with 'minicore' regions of sarcomeric disorganization, lack of oxidative activity, and absent mitochondria

•

en:edema reoccurs with infections

•

en:vacuoles appear to be exocytosing material at the cell surface

•

en:myopathy (in some patients)

•

en:muscle weakness, distal, particularly affecting the hands

•

en:muscle biopsy shows type 1 fiber predominance

•

en:proximal muscle weakness, mild (in some patients)

•

en:muscle biopsy shows necrotic and regenerating fibers

•

en:degrading mitochondria

•

en:motor clumsiness

•

en:distal muscle weakness, predominantly lower limbs

•

en:symptoms are progressive for a few years, and then become stationary

•

en:distal limb muscle weakness occurs later

•

en:paracrystalline inclusions

•

en:increased lipid

•

en:upper limb muscle weakness may be more severe than lower limb weakness

•

fasciculation d'un muscle squelettique

•

en:cerebral abscess

•

en:spasticity (later onset)

•

en:stimulation sensitive generalized myoclonus (stage 3)

•

en:spastic-ataxic tetraparesis

•

hypoplasie glutéale

•

en:small but structurally normal cerebral cortex

•

en:muscle biopsy shows lipid deposition

•

en:muscle biopsy shows mild dystrophic changes

•

en:atrophy of neck muscles may occur later

•

en:hip abductor weakness and atrophy

•

en:z-line streaming see on electron microscopy

•

en:spastic diplegia, symmetric

•

en:muscle weakness of the face and neck, mild to moderate

•

en:loss of gluteal adipose tissue

•

en:muscle atrophy restricted to the upper limb

•

en:muscle biopsy shows chronic and active denervation

•

en:distal muscle atrophy due to denervation

•

en:shoulder weakness

•

en:weakness of ankle and toe extensor (dorsiflexor) muscles

•

en:increased centralized nuclei

•

en:triceps aplasia

•

en:poor muscle mass

•

en:loss of subcutaneous adipose tissue from upper limbs and trunk

•

en:muscle biopsy shows fiber type disproportion

•

en:myotonia improves with continued activity ('warm-up phenomenon')

•

en:exercise intolerance (also seen in some heterozygotes)

•

en:inclusions form a lobulated structure seen on electron microscopy

•

en:increased fatigue

•

en:fatty replacement

•

en:decreased muscle bulk

•

en:distal muscles may be affected

•

en:distal limb muscle weakness due to peripheral neuropathy (lower limbs are more affected than upper limbs)

•

en:episodic weakness may or may not occur independent of myotonia

•

en:fatty infiltration of affected muscles

•

en:cores or minicores

•

en:benign soft tissue developmental anomalies

•

en:calcific tendinopathy, early-onset (in some patients)

•

en:biceps aplasia

•

en:colpocephaly

•

en:abnormal fat accumulation in the back (in some patients)

•

en:myofibromatosis

•

eye

•

holoprosencéphalie

•

sensation de rotation

•

en:acute cerebrovascular accidents

•

déficit en cytochrome-c oxydase

•

en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy

•

en:congenital absence of gluteal muscles

•

en:attacks precipitated by hypokalemia, administration of glucose or insulin, heavy carbohydrate consumption, stress, fatigue, rest after exercise

•

en:hypoesthesia over affected areas

•

en:infantile axial hypotonia

•

en:neurogenic atrophy

•

en:hypertonia at birth

•

en:lymphography shows increased number of dilated lymphatic vessels (hyperplasia)

•

en:lipid and glycogen accumulation

•

en:hip flexor weakness

•

en:mild kinetic abnormalities of the achr (in some patients)

•

en:wide variation in fiber size

•

en:proximal muscle weakness, limb-girdle distribution

•

en:slowly-progressive muscle wasting and weakness with humeroperoneal and scapuloperoneal distribution

•

en:severe disability within 20 years of onset

•

en:increased endomysial connective tissue around muscle fibers

•

en:sparing of the anterior tibial compartment

•

en:muscle cramps during exercise

•

en:severe muscle wasting and atrophy, primarily in the legs

•

en:nemaline rods (rare)

•

en:ragged-red muscle fibers

•

en:deep finger muscle weakness

•

en:hypotonia, infantile, severe

•

en:muscle biopsy shows abnormal fiber size and variation

•

en:muscle weakness, congenital

•

en:protein aggregates immunopositive for actin and desmin

•

en:paucity or absence of lymph nodes in the axillae and above the inguinal ligaments seen on scintilymphangiography

•

en:hypoglycosylation of alpha-dystroglycan

•

en:limb muscle weakness, proximal, upper and lower

•

en:jitter

•

en:loss of independent ambulation around age 12 years

•

en:disruption plasma membrane (in some patients)

•

en:decreased mitochondrial respiratory activities (in some patients)

•

en:loss of subcutaneous adipose tissue from gluteal region

•

en:muscle weakness, primarily proximal

•

en:plasma membrane discontinuities

•

en:hyperthermia

•

en:repetitive compound muscle action potentials (cmap) in response to single stimulus

•

en:mental deterioration

•

en:abnormality of the musculature of the lower limbs

•

en:leg edema

•

en:proximal myopathy

•

en:muscle hypertrophy

•

en:congenital fiber-type disproportion

•

en:developmental delay

•

en:decreased exercise tolerance

•

en:fibrillation

•

en:autism

•

en:muscular rigidity

•

en:leigh disease

•

en:psychosis

•

en:acute rhabdomyolysis

•

nerf périphérique

•

en:tussive syncopes

•

en:hypotonia

•

en:syncope

•

en:mutism

•

en:profound intellectual disabilities

•

en:stiff gait

•

faiblesse de muscle

•

en:muscle weakness upper limb

•

en:hemiplegic posture

•

en:finding of color of limb

•

en:migraine with aura

•

en:cataplexy

•

en:guillain-barre syndrome

•

en:abnormal fat pad, buttocks and upper thighs (in some patients)

•

en:hydrocephalus (variable)

•

en:increased glycogen in muscle (but to a lesser extent than in the heart)

•

en:ragged red fibers, mainly in type i fibers seen on skeletal muscle biopsy

•

en:decreased muscle bulk (in one patient)

•

en:abnormal size and shape of synaptic endplates

•

en:increased white matter signal

•

en:bifrontal subdural hygroma

•

en:motor neuron disease

•

en:mood lability

•

syndrome du sinus carotidien

•

paralysie générale

•

encéphalopathie hépatique

•

en:progressive encephalopathy

•

en:head titubation

•

en:hematomas, recurrent large subcutaneous

•

en:progressive peripheral neuropathy

•

moelle épinière

•

en:neck muscle weakness

•

en:intercostal muscle weakness

•

en:focal dystonias

•

en:decreased activity of mitochondrial complex i

•

en:dysplastic cerebellar gangliocytoma

•

neuropathie

•

en:nodular heterotopia

•

en:ventriculomeglia

•

en:cerebral cyst

•

en:movement of visual image - finding

•

en:inability to jump or squat

•

dysphagia

•

en:abdominal wall muscle weakness (later onset)

•

moelle spinale

•

être en diminution

•

maladie de refsum

•

en:babinski sign

•

en:muscle atrophy, lower limbs more affected than upper limbs

•

tremblement essentiel

•

en:essential tremor

•

substance blanche

•

en:impaired vibration sense

•

en:narcolepsy

•

état vertigineux

•

choc cardiogène

•

fièvre

(médecine)

•

en:fall on the ground

•

yeux

•

en:muscle twitch

•

secousse musculaire

•

en:empty sella syndrome

•

en:gait disturbance

•

maladie de Refsum

•

en:small hippocampi (1 patient)

•

en:spasticity may be present

•

en:muscle biopsy shows loss of myofibrillar organization

•

en:spasticity, mainly in the lower limbs

•

en:spasticity in infancy (1 patient)

•

en:speech absent or delayed

•

tomber par terre

•

en:to rain cats and dogs

•

en:spongy gliosis

•

pâmoison

•

en:abnormal mitochondria

•

en:crick in your neck

•

s'amenuiser

•

amenuiser quelque chose

•

en:aciclovir

•

en:face ague

•

en:familial tremor

•

en:rain dogs and cats

•

myotonie

•

hypo-esthésie

•

en:retardation

•

asphyxia

•

en:auditory auras

•

pleuvoir des cordes

•

en:distal upper limb muscle weakness

•

Maladie de Refsum

•

au noir

•

en:meninx

•

hypothyroïdie (manifestations neuromusculaires dans l')

•

paraplégie spastique avec atrophie optique et démence

•

en:pars centralis systemae nervosi

•

en:choristoma

•

tomber des hallebardes

•

nerf moteur oculaire externe

•

en:to fall flat on one's face

•

en:brain haemorrhage

•

en:some patients have neurologic involvement

•

en:go arse over tit

•

en:speech deterioration

•

en:biceps brachii atrophy

•

en:small, angulated muscle fibers seen on muscle biopsy

•

en:distal muscle atrophy, affecting the lower limbs

•

en:normal neonatal period may occur before weakness is apparent

•

en:muscle biopsy shows nonspecific myopathic changes without dystrophic or inflammatory changes

•

en:muscle fiber necrosis

•

en:small rounded fibers

•

en:proliferation of fatty tissue in muscle (in some patients)

•

en:lymphedema of upper and/or lower limbs (in some patients)

•

en:atrophy of the small muscles in the hands and feet

•

en:proximal upper limb amyotrophy

•

en:hypotonia, truncal and appendicular

•

en:hip girdle muscle atrophy

•

en:muscle biopsy shows myopathic or dystrophic changes

•

en:variation of myofiber diameter

•

en:loss of ambulation (in some patients)

•

en:inability to stand on tiptoes

•

en:granular deposits in the sarcomeres

•

en:hypoplasia of serratus anterior muscle

•

en:variability in fiber size

•

en:hyaline inclusion

•

en:weakness of neck extensors (rare)

•

en:generalized muscle weakness also seen in symptomatic carrier females

•

en:swelling of the affected areas

•

en:decreased caveolin-3 expression seen on muscle biopsy

•

en:independent walking may not be achieved

•

en:mitochondria are placed at the periphery of muscle fibers

•

en:dystrophic changes

•

en:distal muscle weakness and atrophy, upper and lower limbs

•

en:edema (hands and feet)

•

en:abnormal mitochondrial proliferation

•

en:myotonia is most pronounced in the extremities

•

en:subsarcolemmal accumulation of normal mitochondria (in some patients)

•

en:increased variation in fiber size seen on muscle biopsy

•

en:decreased muscle action potential after warming affected muscle

•

en:mild decrease in mitochondrial respiratory chain activity

•

en:limb-girdle muscle atrophy

•

en:centralized myonuclei

•

en:generalized amyoplasia

•

en:muscle biopsy may show deficiency of multiple mitochondrial respiratory complexes

•

en:type 2 fiber atrophy see on biopsy

•

en:myotonia is usually not seen

•

en:muscle weakness and atrophy, distal

•

en:muscle weakness (in some patients)

•

en:exercise-induced muscle stiffness

•

en:muscle biopsy shows groups of small angulated fibers consistent with denervation

•

en:symmetrical muscle wasting

•

en:fiber-type variability

•

en:muscle wasting due to chronic denervation

•

en:increased perisarcolemmal calcium deposition

•

en:lipoatrophic appearance

•

en:structurally abnormal mitochondria

•

en:transient neonatal hypotonia (less common)

•

en:proximal muscle weakness, less severe

•

en:proximal muscle weakness occurs later

•

en:hypoglycosylation of alpha-dystroglycan seen on muscle biopsy

•

en:heterotopic bone formation in subcutaneous fat

•

en:foot dorsiflexor weakness

•

en:lymphedema of the lower limbs (swelling is confined to below the knees)

•

en:intermyofibrillar and subsarcolemmal accumulation of electron-dense material (in some patients)

•

en:minicore regions are poorly defined and do not extend through entire fiber length

•

en:mitochondria show paracrystalline inclusions

•

en:muscle hypertrophy of the lower extremities

•

en:muscle biopsy shows grouped atrophy

•

en:muscle weakness, predominantly proximal

•

en:decreased shank muscle mass

•

en:calf hypertrophy (reported in 1 family)

•

en:humeroperoneal weakness and atrophy

•

en:bilateral facial weakness (congenital form)

•

en:difficulty raising arms

•

en:finger and wrist extensor weakness

•

en:decreased postsynaptic length

•

en:dystrophic changes occur later

•

en:hand and foot weakness

•

en:decreased adipose tissue around neck

•

en:attacks precipitated by potassium

•

en:decreased distal reflexes

•

en:distal muscle weakness and atrophy may occur, upper and lower limbs affected

•

en:centralized nuclei, rare

•

en:fat pad anterior to malleolus

•

en:distal amyotrophy (hands and feet)

•

en:muscle fiber regeneration

•

en:changes in sarcoplasmic reticulum and t-tubules

•

en:distal muscle weakness (first affects anterior leg muscles, then posterior leg muscles)

•

en:marked muscular hypertrophy

•

en:sparing of anterior tibialis muscle

•

en:congenital myasthenic syndrome (reported in 1 patient who survived to age 20 years)

•

en:distal muscle weakness and atrophy of upper and lower limbs due to peripheral neuropathy

•

en:subsarcolemmal accumulation of enlarged mitochondria with variably sized rectangular or elongated rhomboidal paracrystalline inclusions

•

en:cores have abrupt borders within normal regions of the muscle fiber

•

en:difficulty walking up stairs

•

en:biopsy shows rimmed vacuoles, central nuclei, and variation in fiber size

•

en:small, firm, rubbery, flesh-colored nodules most commonly found on the head, neck, and trunk

•

en:muscle weakness, proximal and distal

•

en:biopsy shows myopathy without vacuoles

•

en:merosin-positive biopsy

•

en:hyaline plaques with absent oxidative activity

•

en:secondary myopathic features

•

en:symptoms may be induced by heat

•

en:muscle fiber splitting (in some patients)

•

en:rhabdomyolysis (in some patients)

•

en:quadriceps atrophy (later onset)

•

en:painful swelling in aponeuroses

•

en:normal or increased truncal adipose tissue

•

en:loss of subcutaneous and visceral adipose tissue, mild

•

en:minipolymyoclonus

•

en:myxedematous appearance

•

en:fiber-type grouping pattern

•

en:calf pseudohypertrophy rare

•

en:absence of telethonin protein

•

en:electromyographic decrements in some muscles

•

en:muscle biopsy shows decreased activity of cytochrome c oxidase

•

en:muscle aches, cramps

•

en:contractures of upper limbs (in some patients)

•

en:acute poliomyelitis

•

en:decreased muscle mass

•

en:fasciculation

•

oedème

•

encéphalopathie

•

en:neuropathy

•

en:schizophrenia

•

en:fine tremors

•

en:broad-based gait

•

en:astrocyte

•

en:anxiety

•

en:central nervous system

•

en:polymyositis

•

en:paresis as late effect of poliomyelitis

•

en:exercise-induced myalgia

•

en:frontotemporal dementia

•

en:weakness of upper extremities

•

tic douloureux

•

Fothergill

•

en:trigeminal neuralgia

•

en:somnolence

•

en:skin photosensitivity

•

en:spinal cord disorder

•

en:finding of gross movement of limb

•

en:skin folds visible on edematous limb

•

poliomyélite aigüe

•

en:spastic paraplegia

•

en:distal muscle atrophy (1 patient)

•

faiblesse des membres

•

en:poor head control

•

en:gliosis

•

détérioration intellectuelle

•

en:decreased quantal release

•

astrocyte

•

brain

•

sensation vertigineuse

•

apoplexie

•

en:muscular dystrophy (in 1 of 3 patients)

•

en:fat droplets in sarcoplasm and mitochondria seen on skeletal muscle biopsy

•

en:shortened open channel duration

•

en:preserved junctional folds

•

en:hypotonia, profound

•

en:muscle biopsy shows neurogenic atrophy (1 patient)

•

en:increased variation in fiber size (in some patients)

•

en:decreased atp production

•

en:muscle weakness, lower limbs (patient a)

•

en:demyelination

•

en:nonspecific myopathy seen on biopsy

•

en:thinly myelinated axons

•

en:fiber type variation

•

en:cerebral ventriculomegaly

•

en:absent moro response

•

en:limited walking ability

•

en:efferent neuron

•

en:cobblestone lissencephaly

•

syncope due à la chaleur

•

en:cardiogenic shock

•

encéphalopathie hépato-cérébrale

•

en:white matter

•

en:oculomotor apraxia

•

en:decreased muscle succinate dehydrogenase

•

en:increased fatty and connective tissue in skeletal muscle

•

en:axial weakness

•

en:to go down

•

en:electroencephalogram abnormal

•

tomber en décrépitude

•

en:fall into ruin

•

en:sympatic nerve

•

arriération mentale

•

en:power outage

•

en:to come a cropper

•

tomber en miettes

•

en:fall flat on one's face

•

en:congophilic staining

•

en:Babinski sign

•

s'afficher en baisse

•

se baisser

•

maladie de Trousseau

•

en:hydrencephalus

•

ganglion spinal

•

en:fall over

•

en:generalized lack of subcutaneous fat

•

démyélinisation

•

tremblement héréditaire bénin

•

en:white substance

•

en:spinal hemiparesis

•

épiphyse

•

accès fébriles

•

en:hypesthesia

•

convulsions fébriles

•

en:drowsiness

•

en:stiff neck

•

hypotonie

•

black-blanc-beur

•

illicitement

•

mouiller à seaux

•

en:pay for itself

•

?dème

•

en:water thesaurismosis

•

en:brainware

•

en:supraclavicular fat pads

•

arriération

•

en:deaf-muteness

•

tomber à plat ventre

•

en:intracranial hemorrhage

•

incapable de marcher

•

en:brain imaging shows supratentorial and infratentorial atrophy

•

en:deaf muteness

•

en:mental deficiency

•

en:off the books

•

pleuvoir des hallebardes

•

congestion cérébrale

•

dysautonomie végétative

•

holoprosencéphalie de type 3

•

en:orthostatic low blood pressure

•

hypotonie, obésité et incisives proéminentes

•

en:leukoencéphalopathy

•

névropathie

•

oligophrénie

•

en:general paralysis

•

en:paraplegia

•

diminution de la sensibilité

•

en:autumn

•

en:decremental compound muscle action potential on repetitive stimulation

•

en:sarcoplasmic inclusions

•

en:pelvic girdle muscle weakness (occurs earlier)

•

en:proximal lower limb amyotrophy

•

en:skeletal muscle biopsy shows dystrophic changes

•

en:areflexia due to muscle weakness

•

en:nuclear clumps

•

en:myopathic changes seen on biopsy

•

en:muscle weakness after cooling or on warming affected muscle

•

en:difficulty in toe walking

•

en:muscle weakness, distal, restricted to the lower limbs

•

en:mild variability in muscle fiber size

•

en:disorganized myofilaments seen on muscle biopsy

•

en:nonspecific muscle fiber atrophy

•

en:increased variability in muscle fiber diameter

•

en:proximal muscle weakness, mild

•

en:muscle atrophy, diffuse, severe

•

en:extensor muscle weakness more severe than flexor muscle weakness

•

méningiome angiomateux

•

en:increased endomysial fibrosis

•

en:exercise-induced weakness

•

en:easy fatigue

•

en:decreased activity of cytochrome c oxidase in most cases seen on muscle biopsy

•

en:generalized muscle contractions, episodic

•

en:autophagosome

•

en:absence of necrosis

•

en:attacks last 4 to 24 hours

•

en:transient muscle weakness occur in 75% of patients, particularly in the arms and hands

•

en:wasted lower leg muscles

•

en:electron microscopy shows subsarcolemmal accumulations of abnormally shaped mitochondria

•

en:muscle biopsy shows cytochrome c oxidase-negative fibers

•

en:weakness and wasting of the lower limbs

•

en:inclusion body myopathy

•

en:spasticity (in some patients)

•

en:muscle biopsy shows myofibrillar myopathy

•

en:proximal muscle weakness in upper limbs

•

en:muscle mitochondria normal by histochemical analysis

•

en:weakness of the muscles in the anterior compartment of the lower leg (particularly the tibialis anterior muscle)

•

en:muscle atrophy in the limbs

•

en:myopathic episodes triggered by exercise, fasting, infection, cold temperatures

•

en:abnormal fat distribution

•

en:stiffness (uncommon)

•

en:tendinous and tuberous xanthoma

•

en:muscle weakness is predominantly of extremities and tongue

•

en:tetanus-like muscle contractions

•

en:thin filament shortening and disorganization (in some patients)

•

en:no lipodystrophy in face and neck

•

en:nemaline bodies

•

en:increased muscle tone (early in life)

•

en:skeletal muscle weakness

•

en:uterine muscle may be stiff during pregnancy

•

en:loss of subcutaneous adipose tissue primarily in gluteal region and lower limbs

•

en:mild weakness of the small hand muscles

•

en:small and incompletely fused muscle fibers seen on biopsy

•

en:skeletal muscle biopsy shows impaired respiratory oxidation

•

en:presynaptic defect at the neuromuscular junction

•

en:progression to proximal muscle weakness

•

en:low muscle mass

•

en:preservation of visceral, neck, and axillary fat pads

•

dystrophie choriorétinienne, ataxie spinocérébelleuse, et hypogonadisme hypogonadotrophique

•

en:stop working

•

hémiparésie

•

hypoplasie du nerf optique bilatérale et familiale

•

parésie spastique-glaucome-retard mental

•

en:wryneck

•

en:infarctus

•

prendre une gamelle

•

tomber des cordes

•

en:grey matter

•

se projeter

•

en:Pineal gland

•

hémorragie cérébrale

•

en:fall on the floor

•

handicap moteur

•

tomber en ruine

•

panne d'électricité

•

cécité

•

en:to crumble into ruin

•

en:bucket down

•

en:disseminated sclerosis

•

rétinite pigmentaire, surdité, retard mental, et hypogonadisme

•

méningoencéphalite

•

s'étriquer

•

en:oligophrenia

•

en:dumbness

•

en:prosoponeuralgia

•

en:deterioration of intellect

•

en:to fall to bits

•

Syndrome de la queue de cheval

•

en:immobility

•

astroglies

•

en:learning disability

•

en:profound deafness

•

ramasser une gamelle

•

tomber de tout son long

•

hémorragie encéphalique

•

Méningite

•

en:cerebrospinal fluid glucose decreased

◀

Génériques

[F] [H]

›

en:muscle weakness

•

en:muscle

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

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=6852049 • caches: c1=12 c2=1007 c3=1

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