Spinocerebellar ataxia type 13
MONDO:0011529Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia.
Also known as: SCA13, spinocerebellar ataxia type 13, autosomal dominant cerebellar ataxia with intellectual disability, autosomal dominant cerebellar ataxia with mental retardation, cerebellar ataxia, autosomal dominant with intellectual disability, cerebellar ataxia, autosomal dominant with mental retardation, spinocerebellar ataxia 13
19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 13 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →-
Can intense walking training help brain injury patients walk better?
Symptom relief Not yet recruitingThis study looks at whether high-intensity walking training can help people with cerebellar damage (a part of the brain that controls balance and coordination) improve their walking ability. Twenty participants will either do intense walking exercises or standard training. The go…
Sponsor: Indiana University • Aim: Symptom relief
Last updated Jun 27, 2026 13:01 UTC
-
AI vs. experts: can a computer judge speech as well as a human?
Knowledge-focused Not yet recruitingThis study will compare how well an AI program (Blings) measures speech clarity in 40 adults with speech disorders from stroke or other neurological conditions. Two speech therapists will also rate the same speech samples. The goal is to see if the AI can reliably replace or assi…
Sponsor: Pusan National University Yangsan Hospital • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:11 UTC