Vertaling van "Progressive tapetochoroidal atrophy " (Engels → Frans) :

choroideremia [ tapetochoroidal dystrophy | progressive tapetochoroidal dystrophy | progressive choroidal atrophy | progressive tapetochoroidal atrophy | progressive chorioretinal degeneration ]
choroïdérémie [ dégénérescence chorio-rétinienne progressive ]

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

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

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

progressive pallidal atrophy
atrophie pallidale évolutive

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

progressive cerebral atrophy
atrophie cérébrale progressive

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

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