Rosenow E C, Engel A G
Am J Med. 1978 Mar;64(3):485-91. doi: 10.1016/0002-9343(78)90235-8.
During the past nine years 10 patients with the adult form of acid maltase deficiency have been observed at the Mayo Clinic. Three of the adults presented with respiratory failure. In all three the respiratory manifestations dominated the clinical picture and the cause of the respiratory failure (muscle weakness) and the underlying myopathy (glycogen storage disease) were initially unsuspected. Careful evaluation of the respiratory function tests, including the maximal static respiratory pressures, electromyographic examination and histochemical and biochemical studies of muscle biopsy specimens eventually led to the correct diagnosis.
在过去九年里,梅奥诊所观察到10例成年型酸性麦芽糖酶缺乏症患者。其中3名成年患者出现呼吸衰竭。在这3例患者中,呼吸症状主导了临床表现,呼吸衰竭的原因(肌肉无力)和潜在的肌病(糖原贮积病)最初未被怀疑。对呼吸功能测试进行仔细评估,包括最大静态呼吸压力、肌电图检查以及肌肉活检标本的组织化学和生化研究,最终得出了正确诊断。