Cerebrotendinous Xanthomatosis: Report of two cases and a novel genetic mutation in an Indian patient

Cerebrotendinous Xanthomatosis (CTX) is an autosomal recessive disorder of bile acid metabolism manifesting typically with the triad of neurological dysfunction, tendon xanthoma, and early onset cataract. The diagnosis is often missed and delayed as the patients do not manifest all the classical fea...

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Bibliographic Details
Main Authors: Bhupender K. Bajaj, Anand Singh, Kuljeet S. Anand, Jyoti Garg
Format: Article
Language:English
Published: Thieme Medical and Scientific Publishers Pvt. Ltd. 2013-12-01
Series:Journal of Neurosciences in Rural Practice
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Online Access:http://www.thieme-connect.de/DOI/DOI?10.4103/0976-3147.116420

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