A Novel Mutation of the GAA Gene in a Patient with Adult-onset Pompe Disease Lacking a Disease-specific Pathology

作者：Fujimoto Shohei; Manabe Yasuhiro^*; Fujii Daiki; Kozai Yuko; Matsuzono Kosuke; Takahashi Yoshiaki; Narai Hisashi; Omori Nobuhiko; Adachi Kaori; Nanba Eiji; Nishino Ichizo; Abe Koji

来源：Internal Medicine, 2013, 52(21): 2461-2464.

DOI：10.2169/internalmedicine.52.0311

• adult-onset Pompe disease
• alpha-1,4-glucosidase
• acid phosphatase

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%26gt;A (M515K), combined with a previously reported mutation, c. 1309 C%26gt;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.

• 出版日期2013