Autosomal recessive spastic paraplegia type 32

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Autosomal recessive spastic paraplegia type 32

Synonyms: SPG32

Autosomal recessive spastic paraplegia type 32 (SPG32) is a rare complex type of hereditary spastic paraplegia characterized by a slowly progressive spastic paraplegia (with walking difficulties appearing at onset at 6-7 years of age) associated with mild intellectual disability. Brain imaging reveals thin corpus callosum cortical and cerebellar atrophy and pontine dysraphia. The SPG32 phenotype has been mapped to a locus on chromosome 14q12-q21.

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 April 2024

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Autosomal recessive spastic paraplegia type 32?

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Genetic Support Network of Victoria

The Genetic Support Network of Victoria is an organisation that supports people living with genetic, undiagnosed and rare conditions and those who support them including community and families, patient support organisations, health professionals and industry. Our vision is our community flourishing and living their best lives.

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