Saĭkova L A, Lobzin V S
Zh Nevropatol Psikhiatr Im S S Korsakova. 1988;88(3):3-6.
Sixteen patients with congenital myopathies with the onset of the disease in early childhood were examined. All patients were subjected to morphological investigation of biopsy samples of muscle tissue, using histochemical methods for the determination of the activity of redox and glycolysis enzymes. A clinical polymorphism of these forms of myodystrophies and the presence of nondifferentiated variants were established. The distribution of the activities of oxidation and glycolysis enzymes was histochemically different.
对16例在幼儿期发病的先天性肌病患者进行了检查。所有患者均对肌肉组织活检样本进行了形态学研究,采用组织化学方法测定氧化还原酶和糖酵解酶的活性。确定了这些形式的肌营养不良症的临床多态性以及未分化变体的存在。氧化酶和糖酵解酶活性的分布在组织化学上有所不同。