van Riet W, de Meirsman J, de Saedeleer J, Dom R, Carton H, van den Heede J, Bulcke J A
Clin Neurol Neurosurg. 1985;87(2):85-90. doi: 10.1016/0303-8467(85)90102-7.
The authors present a case report of early onset myophosphorylase deficiency (Mc Ardle's disease) with absence of myophosphorylase protein on SDS-electrophoresis. The different varieties of myophosphorylase deficiency and the clinical investigations which may lead to the diagnosis are reviewed. In particular, the relevance and possible dangers of an ischemic forearm exercise test and the suggestion of using a needle biopsy as a preliminary screening in similar cases of metabolic myopathies are discussed.
作者报告了一例早发性肌磷酸化酶缺乏症(麦克尔迪氏病)病例,该病例在十二烷基硫酸钠电泳中未检测到肌磷酸化酶蛋白。文中回顾了肌磷酸化酶缺乏症的不同类型以及可能有助于诊断的临床检查。特别讨论了缺血性前臂运动试验的相关性和潜在风险,以及在类似代谢性肌病病例中使用针吸活检作为初步筛查方法的建议。