X-linked spinocerebellar ataxia type 3 (Q96473): Difference between revisions

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Latest revision as of 12:29, 16 August 2026

X-linked spinocerebellar ataxia type 3 is a form of spinocerebellar degeneration characterised by onset in infancy of hypotonia, ataxia, sensorineural deafness, developmental delay, esotropia, and optic atrophy, and by a progressive course leading to death in childhood.

Language	Label	Description	Also known as
default for all languages	ID_261426817
English	X-linked spinocerebellar ataxia type 3	X-linked spinocerebellar ataxia type 3 is a form of spinocerebellar degeneration characterised by onset in infancy of hypotonia, ataxia, sensorineural deafness, developmental delay, esotropia, and optic atrophy, and by a progressive course leading to death in childhood.