voksen

Wiki Spinal muscular atrophy

wiki Spinal muscular atrophy

Spinal muscular atrophy (SMA), also called autosomal recessive proximal spinal muscular atrophy and 5q spinal muscular atrophy in order to distinguish it from  ‎ Nusinersen · ‎ Hyporeflexia · ‎ Spinal muscular atrophies. Spinal muscular atrophy with progressive myoclonic epilepsy (SMA -PME), sometimes called Jankovic–Rivera syndrome, is a very rare neurodegenerative. Nusinersen (INN), marketed as Spinraza, is the first drug approved by the U.S. In , the spinal muscular atrophy disease-causing gene, termed the survival motor neuron (SMN), was discovered. Each individual has 2 SMN genes, SMN1. Werdnig-Hoffman disease, which is also known as spinal muscular atrophy type 1 (SMA1) or acute spinal muscular atrophy, refers to. Spinal muscular atrophies (SMAs) are a genetically and clinically. wiki Spinal muscular atrophy

Wiki Spinal muscular atrophy - med Djævelen

Please help improve this section by adding citations to reliable sources. Congenital central hypoventilation syndrome. Pseudohypertrophy of the gastrocnemius muscle, musculoskeletal deformities, and respiratory failure can occur.

Facebooktwittergoogle_plusredditpinterestlinkedinmail
Næste side »