Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6041383 | Neuromuscular Disorders | 2012 | 4 Pages |
Abstract
Muscle glycogen storage disease 0 (GSD0) is caused by glycogen depletion in skeletal and cardiac muscles due to deficiency of glycogen synthase 1 (GYS1), which is encoded by the GYS1 gene. Only two families with this disease have been identified. We report a new muscle GSD0 patient, a Japanese girl, who had been suffering from recurrent attacks of exertional syncope accompanied by muscle weakness and pain since age 5Â years until she died of cardiac arrest at age 12. Muscle biopsy at age 11Â years showed glycogen depletion in all muscle fibers. Her loss of consciousness was gradual and lasted for hours, suggesting that the syncope may not be simply caused by cardiac event but probably also contributed by metabolic distress.
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Authors
Sayuri Sukigara, Wen-Chen Liang, Hirofumi Komaki, Tokiko Fukuda, Takeshi Miyamoto, Takashi Saito, Yoshiaki Saito, Eiji Nakagawa, Kenji Sugai, Yukiko K. Hayashi, Hideo Sugie, Masayuki Sasaki, Ichizo Nishino,