Simon M, Fauchet R, Hespel J P, Beaumont C, Brissot P, Hery B, Hita De Nercy Y, Genetet B, Bourel M
Gastroenterology. 1980 Apr;78(4):703-8.
The hypothesis has been advanced that the two genes on chromosome 6 determining idiopathic hemochromatosis are not identical alleles and therefore that the disease is not recessively inherited, but rather that two different genes are involved. A study of 63 families points to: (a) the rarity with which a single hemochromatosis gene finds biochemical expression (in only 1 of 5 cases), as revealed through determinations of serum iron, serum ferritin and the desferrioxamine test; (b) no difference in HLA-antigen marking between genes with and those without biochemical expression: (c) no difference other than that produced by chance in the biochemical expression of the two genes in families; and (d) the finding in one highly informative family of identical expression of the two genes. It is concluded that idiopathic hemochromatosis is determined by two homologous alleles in accordance with the classical mode of recessive inheritance.
有一种假说认为,位于6号染色体上决定特发性血色素沉着症的两个基因不是相同的等位基因,因此该疾病不是隐性遗传,而是涉及两个不同的基因。一项对63个家庭的研究表明:(a) 通过血清铁、血清铁蛋白和去铁胺试验测定发现,单个血色素沉着症基因很少能表现出生化特征(仅5例中有1例);(b) 有生化表现的基因与无生化表现的基因在HLA抗原标记上没有差异;(c) 除了家庭中两个基因的生化表现存在偶然差异外,没有其他差异;(d) 在一个信息丰富的家庭中发现两个基因表现相同。结论是,特发性血色素沉着症是由两个同源等位基因按照经典的隐性遗传模式决定的。