Hereditary spastic paraplegia type 19 (SPG19)
Evidence-based neurology checklist on hereditary spastic paraplegia type 19 (spg19): Genetics This is caused by mutations in chromosome 9q The transmission is autosomal dominant The onset is late It causes a mild HSP phenotype Clinical features Nerve conduction studies (NCS)
Genetics
- This is caused by mutations in chromosome 9q
- The transmission is autosomal dominant
- The onset is late
- It causes a mild HSP phenotype
Clinical features
Nerve conduction studies (NCS)
References
Related checklists
- Hereditary spastic paraplegia type 1 (SPG1)
- Hereditary spastic paraplegia type 2 (SPG2)
- Hereditary spastic paraplegia type 3 (SPG3)
- Hereditary spastic paraplegia type 4 (SPG4)
- Hereditary spastic paraplegia type 5 (SPG5)
- Hereditary spastic paraplegia type 6 (SPG6)
- Hereditary spastic paraplegia type 7 (SPG7)
- Hereditary spastic paraplegia type 8 (SPG8)
- Hereditary spastic paraplegia type 9 (SPG9)
- Hereditary spastic paraplegia type 10 (SPG10)
- Hereditary spastic paraplegia type 11 (SPG11)
- Hereditary spastic paraplegia type 12 (SPG12)
- Hereditary spastic paraplegia type 13 (SPG13)
- Hereditary spastic paraplegia type 14 (SPG14)
- Hereditary spastic paraplegia type 15 (SPG15)
- Hereditary spastic paraplegia type 16 (SPG16)
- Hereditary spastic paraplegia type 17 (SPG17)
- Hereditary spastic paraplegia type 18 (SPG18)
- Hereditary spastic paraplegia type 20 (SPG20)
- Hereditary spastic paraplegia type 21 (SPG21)
- Hereditary spastic paraplegia type 22 (SPG22)
- Hereditary spastic paraplegia type 23 (SPG23)
- Hereditary spastic paraplegia type 24 (SPG24)
- Hereditary spastic paraplegia type 25 (SPG25)
