Baksi A K, Buxton P H, Cochrane P, Hughes R R
Postgrad Med J. 1977 Mar;53(617):161-4. doi: 10.1136/pgmj.53.617.161.
A case of McArdle's disease in a man is described in detail and a less complete study of his family is reported. This patient showed the classical features of McArdle's disease and the diagnosis was confirmed by muscle biopsy. Unlike other reported cases of this disorder, this case showed a normal rise in blood lactate levels on ischaemic exercise. This apparently paradoxical finding is discussed. It is suggested that a normal rise in the level of blood lactate on ischaemic exercise should not exclude myophosphorylase deficiency.
详细描述了一名男性的麦克尔迪氏病病例,并报告了对其家族不太完整的研究情况。该患者表现出麦克尔迪氏病的典型特征,肌肉活检证实了诊断。与该疾病其他已报告病例不同的是,此病例在缺血性运动时血乳酸水平正常升高。讨论了这一明显矛盾的发现。有人提出,缺血性运动时血乳酸水平正常升高不应排除肌磷酸化酶缺乏症。