4微量元素代谢先天错误

David M. Danks
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引用次数: 12

摘要

现在已知在人类、老鼠、狗和牛中存在微量元素运输的遗传性疾病。那些涉及到铜的药物被发现的时间最长,在临床上也最为人所知。在Menkes病、x连锁皮肤松弛症和小鼠的x连锁斑驳突变系列中,可以看到铜缺乏的影响。铜的积累也是有害的,在威尔逊氏病中,在一些贝德灵顿梗犬和有毒的乳鼠中,最初对肝脏造成损害,后来对肾脏和大脑造成损害。锌缺乏症见于肠病性肢端皮炎和母乳中锌缺乏症的妇女所生的早产儿,如在致死性乳鼠中所见。对动物突变体,特别是小鼠突变体的研究有助于理解人类疾病,而对这些疾病中微量元素运输的基本缺陷的识别有助于提高对微量元素营养相关知识的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
4 Inborn errors of trace element metabolism

Genetic disorders of trace element transport are now known in humans, mice, dogs and cattle. Those involving copper have been known longest and are best known clinically. Effects due to copper deficiency are seen in Menkes' disease, in X-linked cutis laxa and in the X-linked series of mottled mutants in the mouse. Copper accumulation is also harmful, causing damage initially to the liver and later to the kidneys and brain in Wilson's disease, in some Bedlington terriers and in toxic milk mice. Zinc deficiency is seen in acrodermatitis enteropathica and in premature babies born to women who seem to secrete milk that is zinc-deficient, as is seen in lethal milk mice. Study of animal mutants, especially mutant mice, is helpful in understanding the human diseases and identification of the basic defects in trace element transport in these diseases is improving knowledge relevant to trace element nutrition.

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