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Dystonia 28

ORPHA:589618· ICD-10 G24.8

Definition

A rare persistent combined dystonia characterized by childhood onset of progressive dystonia typically beginning in the lower limbs and eventually progressing to generalized dystonia with involvement of the upper limbs, trunk, face, and neck. Variable developmental delay and intellectual disability, as well as mild microcephaly, short stature, abnormal eye movements, and slightly dysmorphic facial features have been reported in association.

Prevalence
Unknown
Inheritance
Autosomal dominant
Age of onset
Childhood, Infancy