Simon M, Hespel J P, Fauchet R, Brissot P, Hita de Nercy Y, Edan G, Beaumont C, Genetet B, Bourel M
Nouv Presse Med. 1979 Feb 3;8(6):421-4.
We studied iron overloading and HLA genotype in two families with overt forms of idiopathic haemochromatosis in two successive generations. In each family the spouse of the patient with overt haemochromatosis in the first generation had clinical and laboratory signs of moderate iron overload and a HLA haplotype A3, B14 and A3, B7 respectively--which is frequently associated with the haemochromatosis gene. This specific HLA haplotype had been transmitted to the second generation patient with overt disease, which thus could be considered as having received a haemochromatosis gene from each parent. Although the finding of cases of overt disease in successive generation firstly suggests a dominant transmission the genetical analysis of these families lead to further strong argument in favour of recessive inheritance of idiopathic haemochromatosis.
我们对两个连续两代患有显性特发性血色素沉着症的家族进行了铁过载和HLA基因型研究。在每个家族中,第一代显性血色素沉着症患者的配偶分别有中度铁过载的临床和实验室体征以及HLA单倍型A3、B14和A3、B7,这两种单倍型常与血色素沉着症基因相关。这种特定的HLA单倍型已遗传给第二代显性疾病患者,因此可认为该患者从父母双方各获得了一个血色素沉着症基因。尽管连续两代出现显性疾病病例这一发现首先提示为显性遗传,但对这些家族的遗传学分析进一步有力支持了特发性血色素沉着症为隐性遗传的观点。