Islamova I B
Zh Nevropatol Psikhiatr Im S S Korsakova. 1985;85(3):346-8.
The article is devoted to one of the rare forms of hereditary neuromuscular diseases--Becker-Kiner progressive muscular dystrophy. Blood lipids were determined in nine patients aged 16 to 45 years with Becker-Kiner progressive muscular dystrophy. Profound disorders of the blood lipid metabolism were established which were expressed in hyperbeta-lipoproteinemia, hypertriglyceridemia, and hypercholesterinemia. The examination of these parameters is useful for objective assessment of the given form of progressive muscular dystrophy.
本文致力于研究一种罕见的遗传性神经肌肉疾病——贝克尔-金纳进行性肌营养不良症。对9名年龄在16至45岁之间的贝克尔-金纳进行性肌营养不良症患者的血脂进行了测定。结果发现存在严重的血脂代谢紊乱,表现为β-脂蛋白血症、高甘油三酯血症和高胆固醇血症。对这些参数的检查有助于客观评估这种进行性肌营养不良症的特定类型。