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Inherited movement disorders.

Nutan Sharma·David G Standaert
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Abstract

The inherited movement disorders comprise a rapidly growing category of human disease. Advances in genetics have led to the identification of the gene mutation in Huntington's disease and three different gene mutations, which may lead to Parkinson's disease. In addition, gene mutations have been identified in less common movement disorders including Wilson's disease, Hallervorden-Spatz syndrome, paroxysmal kinesogenic choreoathetosis, neuroacanthocytosis, and some forms of dystonia. This article summarizes what is known about the genetic mutations that cause these movement disorders, as well as the clinical features of each disease and the symptomatic treatments currently available.

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Chromosome AberrationsChromosome MappingChromosomes, Human, XGenes, DominantGenes, RecessiveGenetic MarkersGenetic TestingHumansHuntington DiseaseMovement DisordersSex Chromosome AberrationsTwin Studies as TopicJournal ArticleReview

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Nutan Sharma, David G Standaert. 2002. Inherited movement disorders.. https://doi.org/10.1016/s0733-8619(01)00014-7

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