Hereditary spastic paraplegia type 25 (SPG25)
Evidence-based neurology checklist on hereditary spastic paraplegia type 25 (spg25): Genetics This is caused by mutations in chromosome 6q The transmission is autosomal recessive The onset is in adulthood Clinical features Magnetic resonance imaging (MRI) spine: features
Genetics
- This is caused by mutations in chromosome 6q
- The transmission is autosomal recessive
- The onset is in adulthood
Clinical features
Magnetic resonance imaging (MRI) spine: features
References
Related checklists
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- Hereditary spastic paraplegia type 23 (SPG23)
- Hereditary spastic paraplegia type 24 (SPG24)
