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特发性血色素沉着症:通过对家族成员进行HLA分型证明纯合子与杂合子交配情况。

Idiopathic hemochromatosis: demonstration of homozygous-heterozygous mating by HLA typing of families.

作者信息

Bassett M L, Doran T J, Halliday J W, Bashir H V, Powell L W

出版信息

Hum Genet. 1982;60(4):352-6. doi: 10.1007/BF00569217.

Abstract

In five families with idiopathic (hereditary) hemochromatosis, clinical and biochemical expression of the disease occurred in offspring of probands, suggesting an autosomal dominant mode of inheritance. However, HLA typing of subjects indicated that a homozygous-heterozygous mating almost certainly had occurred in four of the five families, resulting in homozygous offspring. Thus, in these families inheritance of the hemochromatosis trait was best explained in terms of an autosomal recessive or intermediate mode of inheritance. This study demonstrates the value of HLA typing in identifying homozygous-heterozygous matings in hemochromatosis families.

摘要

在五个患有特发性(遗传性)血色素沉着症的家族中,先证者的后代出现了该疾病的临床和生化表现,提示为常染色体显性遗传模式。然而,对这些受试者的HLA分型表明,五个家族中有四个家族几乎肯定发生了纯合子与杂合子的交配,从而产生了纯合子后代。因此,在这些家族中,血色素沉着症特征的遗传最好用常染色体隐性或中间遗传模式来解释。本研究证明了HLA分型在识别血色素沉着症家族中纯合子与杂合子交配方面的价值。

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