Spinocerebellar ataxia type 27
MONDO:0012247Spinocerebellar ataxia type 27 (SCA27) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by early-onset tremor, dyskinesia, and slowly progressive cerebellar ataxia.
Also known as: SCA27, spinocerebellar ataxia type 27, cerebellar ataxia autosomal dominant FGF14-related, cerebellar ataxia, autosomal dominant, Fgf14-related, spinocerebellar ataxia 27
21 clinical trials for this condition and its sub-types, 2 tagged with Spinocerebellar ataxia type 27 itself.
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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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SCA27B study aims to map disease progression in 300 participants
Knowledge-focused Recruiting nowThis study follows 300 people with a rare genetic movement disorder called SCA27B, along with some family members and healthy volunteers, for up to 2 years. Researchers will use exams, digital devices, and blood tests to measure how the disease changes over time. The goal is to f…
Sponsor: University Hospital Tuebingen • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:04 UTC