Autosomal dominant spastic paraplegia type 37

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Autosomal dominant spastic paraplegia type 37

Synonyms: SPG37

A pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait extensor plantar responses brisk tendon reflexes in arms and legs decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients.

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 Data version March 2024

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Autosomal dominant spastic paraplegia type 37?

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