Autosomal recessive spastic paraplegia type 62

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Autosomal recessive spastic paraplegia type 62

Synonyms: SPG62

A pure or complex form of hereditary spastic paraplegia characterized by an onset in the first decade of life of spastic paraperesis (more prominent in lower than upper extremities) and unsteady gait as well as increased deep tendon reflexes amyotrophy cerebellar ataxia and flexion contractures of the knees in some.

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 recessive spastic paraplegia type 62?

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