| Literature DB >> 22490322 |
Valentina Emmanuele1, Luis C López, Luis López, Andres Berardo, Ali Naini, Saba Tadesse, Bing Wen, Erin D'Agostino, Martha Solomon, Salvatore DiMauro, Catarina Quinzii, Michio Hirano.
Abstract
Coenzyme Q(10) (CoQ(10)) deficiency has been associated with 5 major clinical phenotypes: encephalomyopathy, severe infantile multisystemic disease, nephropathy, cerebellar ataxia, and isolated myopathy. Primary CoQ(10) deficiency is due to defects in CoQ(10) biosynthesis, while secondary forms are due to other causes. A review of 149 cases, including our cohort of 76 patients, confirms that CoQ(10) deficiency is a clinically and genetically heterogeneous syndrome that mainly begins in childhood and predominantly manifests as cerebellar ataxia. Coenzyme Q(10) measurement in muscle is the gold standard for diagnosis. Identification of CoQ(10) deficiency is important because the condition frequently responds to treatment. Causative mutations have been identified in a small proportion of patients.Entities:
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Year: 2012 PMID: 22490322 PMCID: PMC3639472 DOI: 10.1001/archneurol.2012.206
Source DB: PubMed Journal: Arch Neurol ISSN: 0003-9942