Hereditary spastic paraplegia type 41 (SPG41)
Evidence-based neurology checklist on hereditary spastic paraplegia type 41 (spg41): Genetics This is caused by mutations in chromosome 11p The transmission is autosomal dominant It usually presents as pure HSP The mean onset age is about 16 years Clinical features
Genetics
- This is caused by mutations in chromosome 11p
- The transmission is autosomal dominant
- It usually presents as pure HSP
- The mean onset age is about 16 years
Clinical features
References
Related checklists
- Hereditary spastic paraplegia type 26 (SPG26)
- Hereditary spastic paraplegia type 27 (SPG27)
- Hereditary spastic paraplegia type 28 (SPG28)
- Hereditary spastic paraplegia type 29 (SPG29)
- Hereditary spastic paraplegia type 30 (SPG30)
- Hereditary spastic paraplegia type 31 (SPG31)
- Hereditary spastic paraplegia type 32 (SPG32)
- Hereditary spastic paraplegia type 33 (SPG33)
- Hereditary spastic paraplegia type 34 (SPG34)
- Hereditary spastic paraplegia type 35 (SPG35)
- Hereditary spastic paraplegia type 36 (SPG36)
- Hereditary spastic paraplegia type 37 (SPG37)
- Hereditary spastic paraplegia type 38 (SPG38)
- Hereditary spastic paraplegia type 39 (SPG39)
- Hereditary spastic paraplegia type 40 (SPG40)
- Hereditary spastic paraplegia type 42 (SPG42)
- Hereditary spastic paraplegia type 43 (SPG43)
- Hereditary spastic paraplegia type 44 (SPG44)
- Hereditary spastic paraplegia type 45 (SPG45)
- Hereditary spastic paraplegia type 46 (SPG46)
- Hereditary spastic paraplegia type 47 (SPG47)
- Hereditary spastic paraplegia type 48 (SPG48)
- Hereditary spastic paraplegia type 49 (SPG49)
- Hereditary spastic paraplegia type 50 (SPG50)
