Autosomal recessive spastic paraplegia type 25

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Autosomal recessive spastic paraplegia type 25

Synonyms: Autosomal recessive spastic paraplegia-disc herniation syndrome | SPG25

Autosomal recessive spastic paraplegia type 25 (SPG25) is a rare complex type of hereditary spastic paraplegia characterized by adult-onset spastic paraplegia associated with spinal pain that radiates to the upper or lower limbs and is related to disk herniation (with minor spondylosis) as well as mild sensorimotor neuropathy. The SPG25 phenotype has been mapped to a locus on chromosome 6q23-q24.1.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024

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