Angelini C, Lücke S, Cantarutti F
Neurology. 1976 Jul;26(7):633-7. doi: 10.1212/wnl.26.7.633.
We studied a 10-year-old girl with an insidious muscle disease beginning at age 7. Muscle biopsy showed that the majority of type I fibers were vacuolated and contained lipid excess. Carnitine deficiency was found in skeletal muscle. The patient was treated with 3.0 gm L-carnitine per day and with a medium-chain triglyceride diet. She showed a rapid improvement and recovery of strength. A muscle biopsy 8 months later showed a decreased lipid content. Oral carnitine replacement represents an effective treatment for the disease.
我们研究了一名10岁女孩,她自7岁起患有一种隐匿性肌肉疾病。肌肉活检显示,大多数I型纤维出现空泡化且脂质过多。在骨骼肌中发现了肉碱缺乏。该患者每天接受3.0克左旋肉碱治疗,并采用中链甘油三酯饮食。她的力量迅速改善并恢复。8个月后的肌肉活检显示脂质含量降低。口服补充肉碱是该疾病的一种有效治疗方法。