Wieacker P, Zimmer J, Ropers H H
Clin Genet. 1985 Sep;28(3):238-42. doi: 10.1111/j.1399-0004.1985.tb00392.x.
For Incontinentia pigmenti Bloch-Sulzberger (IP) and Aicardi syndrome, an X-linked dominant transmission with lethality in hemizygous males has been proposed. The typical transition from inflammation to verrucous hypertrophy and hyperpigmented skin areas in IP suggests a gradual replacement of defective cells by normal cells. This would imply a preferential inactivation of the X chromosome carrying the IP gene with a proliferative advantage of this cell population. We have confirmed this hypothesis by demonstrating that the same X chromosome is preferentially active in fibroblasts grown from normal and hyperpigmented skin of an affected girl. In contrast, X inactivation was random in a girl with Aicardi syndrome.
对于色素失禁症(布洛赫-苏尔茨贝格综合征,IP)和艾卡迪综合征,有人提出其为X连锁显性遗传,半合子男性具有致死性。IP中从炎症到疣状增生和皮肤色素沉着区域的典型转变表明,缺陷细胞逐渐被正常细胞替代。这意味着携带IP基因的X染色体优先失活,而该细胞群体具有增殖优势。我们通过证明在一名患病女孩的正常皮肤和色素沉着皮肤中培养的成纤维细胞中,同一X染色体优先活跃,证实了这一假设。相比之下,一名艾卡迪综合征女孩的X染色体失活是随机的。