Lipid storage myopathies with unusual clinical manifestations.

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dc.contributor.authorUppin, Megha Sen_US
dc.contributor.authorSundaram, Cen_US
dc.contributor.authorMeena, A Ken_US
dc.contributor.authorReddy, Krishna Mohanen_US
dc.contributor.authorReddy, K Krishnaen_US
dc.contributor.authorVanniarajan, Aen_US
dc.contributor.authorThangaraj, Ken_US
dc.date.accessioned2008-07-01en_US
dc.date.accessioned2009-06-03T11:30:21Z
dc.date.available2008-07-01en_US
dc.date.available2009-06-03T11:30:21Z
dc.date.issued2008-07-01en_US
dc.description.abstractWe describe the clinical presentation, course and pathologic findings found in three adult patients with lipid storage myopathy. Excessive lipid storage was found in Type 1 fibers of muscle. Clinical improvement on oral levo-carnitine therapy suggests the possibility of carnitine deficiency as the most likely etiology in two of the patients and one had mitochondrial myopathy confirmed on genetic analysis.en_US
dc.description.affiliationNizam's Institute of Medical Sciences, Hyderabad, India. challa_sundaram@yahoo.com.en_US
dc.identifier.citationUppin MS, Sundaram C, Meena AK, Reddy KM, Reddy KK, Vanniarajan A, Thangaraj K. Lipid storage myopathies with unusual clinical manifestations. Neurology India. 2008 Jul-Sep; 56(3): 391-3en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/120934
dc.language.isoengen_US
dc.source.urihttps://neurologyindia.comen_US
dc.titleLipid storage myopathies with unusual clinical manifestations.en_US
dc.typeJournal Articleen_US
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