Hereditary spastic paraplegia type 89 (SPG89)
Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .
Hereditary spastic paraplegia type 89 (SPG89). This is caused by mutations in the AMFR gene. Fully referenced neurology checklist.
Genetics
- This is caused by mutations in the AMFR gene
- The gene is on chromosome 16
- The transmission is autosomal recessive
Neurological features
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Magnetic resonance imaging (MRI) brain
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References
Related checklists
- Hereditary spastic paraplegia type 76 (SPG76)
- Hereditary spastic paraplegia type 77 (SPG77)
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- Hereditary spastic paraplegia type 82 (SPG82)
- Hereditary spastic paraplegia type 83 (SPG83)
- Hereditary spastic paraplegia type 84 (SPG84)
- Hereditary spastic paraplegia type 85 (SPG85)
- Hereditary spastic paraplegia type 86 (SPG86)
- Hereditary spastic paraplegia type 87 (SPG87)
- Hereditary spastic paraplegia type 88 (SPG88)
