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A prospective series of patients with hyperglycaemia-associated movement disorders

✍ Scribed by Amin Cervantes-Arriaga; Georgina Arrambide; Mayela Rodríguez-Violante

Book ID
116676106
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
322 KB
Volume
18
Category
Article
ISSN
0967-5868

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✍ Cyril Gitiaux; Emmanuel Roze; Kiyoka Kinugawa; Constance Flamand-Rouvière; Natha 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 129 KB

## Abstract Glutaric aciduria type 1 (GA1) is an autosomal recessive neurometabolic disorder due to glutaryl CoA dehydrogenase deficiency. Comprehensive descriptions of GA1‐associated movement disorders are rare. In order to refine the description of the motor phenotype, we prospectively studied 16