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Neuroacanthocytosis: clinical, radiological, and neurophysiological findings in an Italian family

✍ Scribed by A.M. Marson; E. Bucciantini; E. Gentile; C. Geda

Publisher
Springer Milan
Year
2003
Tongue
English
Weight
28 KB
Volume
24
Category
Article
ISSN
1590-1874

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## Abstract Benign hereditary chorea is an autosomal dominant disorder characterized by early onset nonprogressive chorea, caused by mutations of the __thyroid transcription factor‐1 (TITF‐1)__ gene. Clinical heterogeneity has been reported and thyroid and respiratory abnormalities may be present.