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[Infantile spinal muscular atrophy].
A Barois1, B Estournet, G Duval-Beaupère
1Service de Réanimation Infantile, Hôpital Raymond Poincaré, Garches.
Revue Neurologique
|January 1, 1989
Summary
This study examines 100 individuals with prolonged spinal muscular atrophy (SMA), detailing their survival, ambulatory capabilities, and disease progression. Findings support the unified classification of SMA types and highlight varied outcomes based on symptom onset and ambulatory status.
Area of Science:
- Neurology
- Genetics
- Pediatrics