Journal
INTERNAL MEDICINE
Volume 52, Issue 21, Pages 2461-2464Publisher
JAPAN SOC INTERNAL MEDICINE
DOI: 10.2169/internalmedicine.52.0311
Keywords
adult-onset Pompe disease; alpha-1,4-glucosidase; acid phosphatase
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We herein report a novel compound heterozygous mutation of the acid a-glucosidase (GAA) gene in a 23-year-old man with adult-onset Pompe disease. The patient was admitted for respiratory failure and a highly elevated serum level of creatine kinase (CK). His muscle pathology did not show typical vacuolated fibers; however, globular inclusion bodies with acid phosphatase (ACP) activity was observed. A molecular genetic analysis of the GAA gene revealed a novel compound heterozygous mutation, c. 1544 T>A (M515K), combined with a previously reported mutation, c. 1309 C>T (R437C). The presence of ACP-positive globular inclusion bodies is a useful diagnostic marker for adult-onset Pompe disease, even when typical vacuolated fibers are absent.
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