Hereditary spastic paraplegia type 38 (SPG38)
Evidence-based neurology checklist on hereditary spastic paraplegia type 38 (spg38): Genetics This is caused by mutations in chromosome 4p The transmission is autosomal dominant It is allelic with SPG4 It is similar to Silver syndrome Clinical features
Genetics
- This is caused by mutations in chromosome 4p
- The transmission is autosomal dominant
- It is allelic with SPG4
- It is similar to Silver syndrome
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 39 (SPG39)
- Hereditary spastic paraplegia type 40 (SPG40)
- Hereditary spastic paraplegia type 41 (SPG41)
- 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)
