Bicarnesine-treated carnitine deficient myopathy: clinico-chemical investigations.

Acta paediatrica Hungarica Pub Date : 1992-01-01
A László, L Klujber, A Svékus
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Abstract

Authors report on a Bicarnesine replacement therapy in an infant girl patient suffering from carnitine deficient myopathy diagnosed at 1 year of age. The hypotonic patient's motoric functions improved and she became able to walk as a result of therapy applied, but the pathological process generalized to encephalomyopathy. Free and esterified carnitine were determined from the serum and muscle biopsymaterial. After the Bicarnesine-supplementation the serum carnitine fractions elevated.

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比卡尼斯治疗肉碱缺乏性肌病:临床化学研究。
作者报告了一名患有左旋肉碱缺乏性肌病的女婴患者在1岁时诊断的比卡尼辛替代疗法。治疗后,低张力患者的运动功能得到改善,并能行走,但病理过程发展为脑肌病。从血清和肌肉活检材料中测定游离肉碱和酯化肉碱。补充比卡尼斯后,血清肉碱含量升高。
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