SPINOCEREBELLAR ATAXIA TYPE 27B

Clinical trials for SPINOCEREBELLAR ATAXIA TYPE 27B explained in plain language.

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SCA27B study aims to map rare movement Disorder's progression

Knowledge-focused Recruiting now

This study follows 300 people with a rare genetic movement disorder called SCA27B, along with some family members and healthy volunteers, for two years. Researchers will track changes in balance, coordination, and other symptoms using exams, digital tools, and lab tests. The goal…

Matched conditions: SPINOCEREBELLAR ATAXIA TYPE 27B

Sponsor: University Hospital Tuebingen • Aim: Knowledge-focused

Last updated Apr 30, 2026 15:51 UTC

SPINOCEREBELLAR ATAXIA TYPE 27B

Get alerted when new SPINOCEREBELLAR ATAXIA TYPE 27B trials appear

SCA27B study aims to map rare movement Disorder's progression