Articles with "kcna1 gene" as a keyword



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Interictal Headache, Pseudodystonia, and Persistent Ataxia in Episodic Ataxia Type 1 Due to a Novel KCNA1 Gene Mutation

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Published in 2022 at "Movement Disorders Clinical Practice"

DOI: 10.1002/mdc3.13381

Abstract: We report a case to broaden our understanding of the unusual phenotypical spectrum of rare genetic ataxia. A 33-year old woman presented with intermittent episodes of periorbital twitching for the last 30 years and episodic… read more here.

Keywords: kcna1 gene; dizzy spells; ataxia; mutation ... See more keywords