| Literature DB >> 28630220 |
Roberto López-Blanco1,2,3, Ana Rojo-Sebastián3, Maria Henedina Torregrosa-Martínez3, Alberto Blazquez4.
Abstract
Madelung's disease (benign symmetric lipomatosis) is a rare syndrome in which there are multiple lipomas around the neck, upper limbs and trunk in the context of chronic alcoholism. We report on a female patient with lipomas and slightly progressive myoclonus, neuropathy, myopathy, ataxia and respiratory systemic involvement (labelled in the past as Madelung's disease). Multisystem involvement and family history of lipomas led to the development of mitochondrial genetic tests, which can assess two concurrent mitochondrial mutations: the m.8344A>G mutation in MT-TK gene, related MERRF (myoclonic epilepsy with ragged-red fibre) phenotype and m.14484T>C mutation in the MT-ND6 gene responsible for Leber hereditary optic neuropathy phenotype. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: Movement disorders (other than Parkinsons); Neuro genetics; Neuromuscular disease; Visual pathway
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Year: 2017 PMID: 28630220 PMCID: PMC5534751 DOI: 10.1136/bcr-2016-218861
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X