Boost Your Productivity!Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
https://pro.wordscope.com
https://blog. wordscope .com
Aran-Duchenne disease
Circumpapillary choroid atrophy
Circumpapillary choroiditis
Cruveilhier disease
Infantile spinal muscular atrophy
PMA
Progressive muscular atrophy
Progressive muscular atrophy of infancy
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 choroidal atrophy » (Anglais → Français) :

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


circumpapillary choroid atrophy | circumpapillary choroiditis

choroïdose circumpapillaire


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


A rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease with characteristics of childhood to adulthood-onset of progressive, moderate to severe, predominantly distal, mostly lower limb muscle weakness and atrophy, foot de

maladie de Charcot-Marie-Tooth intermédiaire autosomique récessive type C


A rare hereditary motor and sensory neuropathy disorder with characteristics of the typical CMT phenotype (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante type F


w