Autosomal dominant spastic paraplegia type 9B

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Autosomal dominant spastic paraplegia type 9B

Synonyms: AD-SPG9B

A rare predominantly pure hereditary spastic paraplegia characterized by juvenile or adult onset of slowly progressive spastic paraparesis gait disturbances and increased tendon reflexes. Additional variable manifestations include pes cavus dysarthria sensory impairment and urinary symptoms. Cognition is normal.

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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Autosomal dominant spastic paraplegia type 9B?

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