Spinocerebellar ataxia 13
A hereditary autosomal dominant spinocerebellar ataxia with onset typically between 20 and 40 years of age. It is characterized by progressive childhood-onset cerebellar GAIT ATAXIA associated with cerebellar DYSARTHRIA, moderate INTELLECTUAL DISABILITY. Associated with mutations in the KCNC3 gene. OMIM: 605259
Also Known As:
Autosomal dominant cerebellar ataxia with mental retardation; Cerebellar ataxia, autosomal dominant with mental retardation; SCA13 Spinocerebellar ataxia 13
Networked: 6
relevant articles (0 outcomes,
0 trials/studies)
Disease Context: Research Results
Related Diseases
Experts
1. | Waters, Michael F:
4 articles
(10/2018 - 03/2011)
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2. | Nick, Harry S:
3 articles
(10/2018 - 01/2013)
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3. | Khare, Swati:
2 articles
(10/2018 - 11/2014)
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4. | Nick, Jerelyn A:
2 articles
(10/2018 - 11/2014)
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5. | Subramony, S H:
2 articles
(10/2018 - 01/2013)
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6. | Pulst, Stefan M:
2 articles
(11/2014 - 03/2011)
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7. | Chan, Chung Yu:
1 article
(01/2022)
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8. | Wu, Ling-Gang:
1 article
(01/2022)
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9. | Galeano, Kira:
1 article
(10/2018)
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10. | Kaczmarek, Leonard K:
1 article
(10/2018)
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Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Spinocerebellar ataxia 13: