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Early-onset generalized dystonia

MONDO:0100016

A generalized isolated dystonia characterized by early-onset, which may be clinically indistinguishable from DYT-TOR1A and may be the most common cause of early-onset generalized dystonia, at least outside the Askenazi Jewish population.

Also known as: DYT-KMT2B, early-onset, generalised dystonia with mild syndromic features, early-onset, generalized dystonia with mild syndromic features, early-onset generalised isolated dystonia, early-onset generalized isolated dystonia

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

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Sub-types

Early-onset generalized limb-onset dystonia (2) Torsion dystonia with onset in infancy (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) Isolated dystonia (4) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)
Trials to join now! 13 Completed 4
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