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Aran-Duchenne disease
Charcot-Marie-Tooth disease
Cruveilhier disease
Disease Charcot-Marie-Tooth
Déjerine-Sottas
Erb's disease
Erb-Landouzy disease
Idiopathic muscular atrophy
Infantile spinal muscular atrophy
Myodystrophia
PMA
PPS
Peroneal muscular atrophy
Post-polio syndrome
Postpolio progressive muscular atrophy syndrome
Postpolio syndrome
Progressive muscular atrophy
Progressive muscular atrophy of infancy
Progressive muscular dystrophy
Progressive neuromuscular atrophy
Progressive spinal muscular atrophy
SMA
SMA I
SPMA
Severe infantile spinal muscular atrophy
Spinal muscular atrophy
Spinal muscular atrophy type I
Spinal progressive muscular atrophy
Werdnig-Hoffman disease

Traduction de «progressive muscular atrophy infancy » (Anglais → Français) :

infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]

amyotrophie spinale infantile sévère | amyotrophie spinale progressive de type I | atrophie spinale progressive infantile | maladie de Werdnig-Hoffmann | syndrome de Werdnig-Hoffmann


Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]

amyotrophie d'Aran-Duchenne | amyotrophie spinale progressive | atrophie de Cruveilhier | atrophie musculaire progressive d'Aran | maladie d'Aran-Duchenne


post-polio syndrome [ PPS | postpolio progressive muscular atrophy syndrome | postpolio syndrome ]

syndrome de post-poliomyélite


progressive muscular dystrophy | Erb-Landouzy disease | Erb's disease | idiopathic muscular atrophy | myodystrophia

myopathie primitive progressive | dystrophie musculaire progressive | myopathie atrophique progressive | amyotrophie primitive progressive | amyotrophie progressive | atrophie musculaire progressive


Charcot-Marie-Tooth disease | peroneal muscular atrophy | progressive neuromuscular atrophy

maladie de Charcot-Marie | syndrome de Charcot-Marie | atrophie de Charcot-Marie | atrophie péronière | amyotrophie de Charcot-Marie-Tooth


A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hyp

myopathie liée à l'X avec atrophie des muscles posturaux


progressive spinal muscular atrophy

atrophie musculaire progressive


Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome

Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy


A rare autosomal recessive distal hereditary motor neuropathy with characteristics of slowly progressive muscular weakness, hypotonia and atrophy of the lower limbs, more pronounced distally, leading to paralysis, and loss of tendon reflexes. Additio

neuropathie motrice distale héréditaire de l'adulte jeune


A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usuall

myopathie à corps d'inclusion héréditaire type 4


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