Hirvioja M L, Kivinen S
Department of Obstetrics and Gynaecology, Kanta-Häme Central Hospital, Hämeenlinna, Finland.
Clin Genet. 1993 Jun;43(6):315-7. doi: 10.1111/j.1399-0004.1993.tb03826.x.
We report three sisters with intrahepatic cholestasis of pregnancy (ICP) and the pedigree of the family, including six generations. ICP was observed in five successive generations; most of the patients also had cholelithiasis. The uniform expression, the complete penetrance of the trait and the direct parent-to-child transmission support the Mendelian dominant mode of inheritance. Determination of HLA A, B and C haplotype was made in five ICP patients, without any findings of HLA type common to everyone. X-linked inheritance cannot be excluded in this study.
我们报告了三例患有妊娠期肝内胆汁淤积症(ICP)的姐妹及其家族谱系,包括六代人。在连续五代人中观察到了ICP;大多数患者还患有胆结石。该性状的一致表达、完全外显率以及直接的亲子传递支持孟德尔显性遗传模式。对五例ICP患者进行了HLA A、B和C单倍型的测定,未发现所有人共有的HLA类型。本研究不能排除X连锁遗传。