Spinocerebellar ataxia type 19 (Q101073): Difference between revisions
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A ataxia espinocerebelar 19 (SCA 19) é um subtipo raro de ataxia cerebelar autossômica dominante tipo I envolvendo um locus no cromossomo 1p21-q21. Caracterizada por ataxia leve, hiporreflexia, mioclonia, tremor postural, comprometimento cognitivo e disfunção do lobo frontal. | |||
| description / en | description / en | ||
Spinocerebellar ataxia 19 (SCA 19) is a rare subtype of type I autosomal dominant cerebellar ataxia involving a locus on chromosome 1p21-q21. Characterized by mild ataxia, hyporeflexia, myoclonus, postural tremor, cognitive impairment, and frontal lobe dysfunction. | |||
Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia 19 (SCA 19) is a rare subtype of type I autosomal dominant cerebellar ataxia involving a locus on chromosome 1p21-q21. Characterized by mild ataxia, hyporeflexia, myoclonus, postural tremor, cognitive impairment, and frontal lobe dysfunction.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1792112140 |
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| English | Spinocerebellar ataxia type 19 |
Spinocerebellar ataxia 19 (SCA 19) is a rare subtype of type I autosomal dominant cerebellar ataxia involving a locus on chromosome 1p21-q21. Characterized by mild ataxia, hyporeflexia, myoclonus, postural tremor, cognitive impairment, and frontal lobe dysfunction. |
