Spinocerebellar ataxia type 23

MONDO:0012449

Spinocerebellar ataxia type 23 (SCA23) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by gait ataxia, dysarthria, slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia.

Also known as: SCA23, spinocerebellar ataxia type 23, spinocerebellar ataxia 23

20 clinical trials for this condition and its sub-types, 1 tagged with Spinocerebellar ataxia type 23 itself.

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Where it sits in the disease tree

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↑ Autosomal dominant cerebellar ataxia type I (16)

Including sub-types (20) Tagged with Spinocerebellar ataxia type 23 (1)

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Could a simple drug stop deadly organ failure after surgery?

Prevention Ongoing

This study tests if a drug called dalargin can prevent serious organ problems like kidney injury, lung failure, or heart damage after major abdominal surgery. About 200 adults having high-risk surgery will get either dalargin or a placebo for 3 days. The goal is to see if dalargi…

Phase 3 • Sponsor: Botkin Hospital • Aim: Prevention

Last updated Jun 27, 2026 09:05 UTC

Spinocerebellar ataxia type 23

Where it sits in the disease tree

Could a simple drug stop deadly organ failure after surgery?