Hayes D J, Summers B A, Morgan-Hughes J A
J Neurol Sci. 1982 Jan;53(1):125-36. doi: 10.1016/0022-510x(82)90086-7.
This paper describes 2 brothers with increasingly severe exercise-induced muscle pain and stiffness, beginning in adolescence. Histochemical studies showed that myoadenylate deaminase activity was absent in the propositus, but present in his younger brother. Biochemical examination of muscle homogenates confirmed these findings, with enzyme activity approximately 60% of the mean control value in the younger sibling. Red cell adenylate deaminase activity was normal in both cases. The possible relationship between the clinical and biochemical findings in these patients is discussed.
本文描述了2名兄弟,自青春期起出现日益严重的运动诱发的肌肉疼痛和僵硬。组织化学研究显示,先证者的肌腺苷酸脱氨酶活性缺失,但其弟弟的该活性存在。肌肉匀浆的生化检查证实了这些发现,弟弟的酶活性约为平均对照值的60%。两例患者的红细胞腺苷酸脱氨酶活性均正常。文中讨论了这些患者临床和生化表现之间可能的关系。