Episodic ataxia type 2
MONDO:0007163A form of hereditary episodic ataxia (EA) characterized by paroxysmal episodes of ataxia lasting hours, with interictal nystagmus and mildly progressive ataxia.
Also known as: CACNA1A hereditary episodic ataxia, episodic ataxia type 2, hereditary episodic ataxia caused by mutation in CACNA1A, APCA, Acetazolamide-responsive episodic ataxia syndrome, Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia, Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia, CAPA
25 clinical trials for this condition and its sub-types.
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Virtual reality could calm anxious kids with autism at the dentist
Symptom relief ENROLLING_BY_INVITATIONThis study tests whether wearing a virtual reality (VR) headset during dental treatment can reduce fear and stress in children with mild intellectual disabilities or autism spectrum disorder. Two hundred children aged 6 to 12 will either receive standard dental care or use a VR h…
Phase: NA • Sponsor: Semmelweis University • Aim: Symptom relief
Last updated Jun 27, 2026 14:02 UTC
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Robot suit helps kids with movement disorders take steps at home
Symptom relief OngoingThis study tests a wearable robotic exoskeleton called EXPLORER in 15 children with movement problems from conditions like cerebral palsy. The goal is to see if it helps them walk better in their everyday environments, such as home and the community. The study focuses on safety, …
Phase: NA • Sponsor: MarsiBionics • Aim: Symptom relief
Last updated Jun 27, 2026 07:51 UTC