Spinocerebellar ataxia 7

*Gene map locus 3p21.1-p12

ADCA, type II

Autosomal dominant cerebellar ataxia, type II

OPCA III

OPCA with macular degeneration and external ophthalmoplegia

OPCA with retinal degeneration

OPCA3

Olivopontocerebellar atrophy III

SCA7

[Clinical features: progressive cerebellar ataxia; pigmentary retinal degeneration]

[Inheritance: autosomal dominant]


Molecular and Clinical Study of Spinocerebellar Ataxia Type 7 in Chinese Kindreds	Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy	Pontine atrophy precedes cerebellar degeneration in spinocerebellar ataxia 7: MRI-based volumetric analysis
Archives of Neurology	European Journal of Human Genetics	Journal of Neurology, Neurosurgery and Psychiatry


Clinical and genetic study of a Chinese family with spinocerebellar ataxia type 7	Clinical and genetic study of a Chinese family with spinocerebellar ataxia type 7	Clinical and genetic study of a Chinese family with spinocerebellar ataxia type 7
Neurology India	Neurology India	Neurology India


Clinical and genetic study of a Chinese family with spinocerebellar ataxia type 7	Fundus of a 34 year-old patient with cone rod dystrophy due to Spinocerebellar Ataxia Type 7 (SCA7)
Neurology India	Orphanet Journal of Rare Diseases

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Edited by Aldo Campana, August 21, 2012