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Spinocerebellar ataxia type 2
MONDO:0008458A subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea.
Also known as: ATXN2 autosomal dominant cerebellar ataxia type I, OPCA2, SCA2, autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2, spinocerebellar ataxia type 2, ALS13, SCA 2, Wadia swami syndrome
38 clinical trials for this condition and its sub-types, 10 tagged with Spinocerebellar ataxia type 2 itself.
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Sub-types of Spinocerebellar ataxia type 2
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Can we predict how genetic ataxias progress?
Knowledge-focused Recruiting nowThis study follows people with several types of spinocerebellar ataxia (SCA) — rare genetic diseases that cause balance, coordination, and speech problems — to learn how these conditions change over time. Researchers will collect blood samples, perform neurological exams, and use…
Sponsor: Lauren Moore • Aim: Knowledge-focused
Last updated Aug 05, 2026 00:00 UTC
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New study sheds light on vision loss in rare genetic brain disorders
Knowledge-focused Recruiting nowThis study looks at how spinocerebellar ataxia (SCA) affects the eyes and vision. Researchers will examine 60 adults with SCA types 1, 2, 3, or 27B, including those with early symptoms and those who are not yet symptomatic. The goal is to measure vision changes and eye damage usi…
Sponsor: University Hospital, Montpellier • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:59 UTC