Autosomal Dominant Proximal Childhood Spinal Muscular Atrophy

mutation in DYNC1H1

Also Known As:

Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant; Kugelberg-Welander Syndrome, Autosomal Dominant; Spinal Muscular Atrophy, Juvenile, Proximal, Autosomal Dominant

Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Nervous System Diseases: 14178
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - Spinal Muscular Atrophies of Childhood: 190
      - Autosomal Dominant Proximal Childhood Spinal Muscular Atrophy