X-linked spinocerebellar ataxia type 3 (Q96473): Difference between revisions
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Ataxia espinocerebelar ligada ao X tipo 3 é uma forma de degeneração espinocerebelar caracterizada por início na primeira infância com hipotonia, ataxia, surdez neurossensorial, atraso no desenvolvimento, esotropia e atrofia óptica, com um curso progressivo que pode levar a óbito na infância. | |||
| description / en | description / en | ||
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. | |||
Revision as of 12:28, 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 |
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| default for all languages | ID_261426817 |
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| 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. |
