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Myoclonus-dystonia syndrome

MONDO:0000903

Myoclonus-dystonia syndrome (MDS) is a rare movement disorder characterized by mild to moderate dystonia along with 'lightning-like' myoclonic jerks.

Also known as: DYT-SGCE, dystonia with myoclonus, hereditary essential myoclonus, myoclonic dystonia, myoclonus-dystonia syndrome, DYT11, Hereditary essential myoclonus, alcohol-responsive dystonia

16 clinical trials for this condition and its sub-types.

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Sub-types

Myoclonic dystonia 11 (0) Myoclonic dystonia 15 (0) Myoclonic dystonia 26 (0)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Movement disorder (89) Dystonic disorder (60) Human disease (14) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2) Combined dystonia (1) Disease by body system or component (0)
Trials to join now! 10 Not yet finished but already full! 1 Completed 5
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  • Global brain surgery matchmaker aims to help kids with rare movement disorders

    Knowledge-focused ENROLLING_BY_INVITATION

    This study is building an online platform called DBS MatchMaker to connect doctors around the world who treat rare movement disorders with deep brain stimulation (DBS). The goal is to help doctors share knowledge and find the best ways to treat patients. Up to 500 people of all a…

    Sponsor: Boston Children's Hospital • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:06 UTC

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