| Literature DB >> 22658436 |
José Luiz Pedroso1, Wladimir B Pinto, Paulo V Souza, Lucas T Santos, Isabela C Abud, Marcela Amaral Avelino, Orlando G Barsottini.
Abstract
Cerebrotendinous xanthomatosis (CTX) is a rare inherited metabolic disorder, which usually presents with diverse systemic manifestations (ophthalmologic, cardiac, and dermatologic symptoms), and neurological dysfunction, such as neuropsychiatric symptoms, cognitive decline, and ataxia. Epilepsy is rarely seen as the main neurological manifestation of CTX. Herein, we describe a middle-aged woman with epilepsy since childhood as the only neurological symptom associated with the classical systemic manifestations of CTX.Entities:
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Year: 2012 PMID: 22658436 DOI: 10.1016/j.yebeh.2012.04.121
Source DB: PubMed Journal: Epilepsy Behav ISSN: 1525-5050 Impact factor: 2.937