1.
Neurol India
;
2008 Jul-Sep; 56(3): 391-3
Article
in English
| IMSEAR
| ID: sea-120934
ABSTRACT
We 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.