Hereditary spastic paraplegia type 16 (SPG16)

Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .

Hereditary spastic paraplegia type 16 (SPG16). This is caused by mutations in chromosome Xq. Fully referenced neurology checklist.

Genetics

  • This is caused by mutations in chromosome Xq
  • The transmission is X-linked

Clinical features

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References

  1. Steinmüller R, Lantigua-Cruz A, Garcia-Garcia R, Kostrzewa M, Steinberger D, Müller U. Evidence of a third locus in X-linked recessive spastic paraplegia. Hum Genet. 1997; 100:287-289. 

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