Hodgson S V, Neville B, Jones R W, Fear C, Bobrow M
Hum Genet. 1985;71(3):231-4. doi: 10.1007/BF00284581.
We report two unrelated girls who present some clinical features of severe incontinentia pigmenti (IP), with characteristic skin pigmentation. Both have balanced de novo X/autosome translocations involving band Xp11. The coincidence of the probable de novo expression of an X-linked disorder in these two girls with translocations involving similar breakpoints on the X chromosome suggests that this band may be the site of the IP gene locus.
我们报告了两名无血缘关系的女孩,她们表现出一些重症色素失禁症(IP)的临床特征及特征性皮肤色素沉着。两人均有涉及Xp11带的平衡型新发X/常染色体易位。这两名女孩患有X连锁疾病且新发表现与X染色体上相似断点的易位同时出现,这表明该带可能是IP基因座的位置。