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Title: LAMP-2 positive vacuolar myopathy with dilated cardiomyopathy. Author: Sugimoto S, Shiomi K, Yamamoto A, Nishino I, Nonaka I, Ohi T. Journal: Intern Med; 2007; 46(11):757-60. PubMed ID: 17541230. Abstract: We report a 46-year-old male patient with late-onset vacuolar myopathy and dilated cardiomyopathy. Acid maltase activity of the muscle was normal, but the biopsied muscle specimen stained for lysosome-associated membrane protein-2 (LAMP-2), which has recently been reported to be deficient in muscles of patients with Danon disease. The clinical features of the patient are distinct from X-linked myopathy with excessive autophagy, infantile autophagic vacuolar myopathy and autophagic vacuolar myopathy with late-onset and multiorgan involvement (Kaneda).[Abstract] [Full Text] [Related] [New Search]