Woffendin H, Jakins T, Jouet M, Stewart H, Landy S, Haan E, Harris A, Donnai D, Read A, Kenwrick S
Department of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
Clin Genet. 1999 Jan;55(1):55-60. doi: 10.1034/j.1399-0004.1999.550110.x.
Familial incontinentia pigmenti (IP) is an X-linked dominant disorder with an extremely variable clinical presentation. Ambiguous diagnosis can complicate genetic counselling and attempts to refine the gene location in Xq28. Marked skewing of X-inactivation patterns is a hallmark of IP and provides a means for investigating uncertain cases. We have conducted X-inactivation studies in three families where Xq28 marker studies were at odds with the original clinical assessment. The results indicate that no recombination between the disease locus and Xq28 loci has occurred and suggest that mosaicism is responsible for the discrepancy in one family.
家族性色素失禁症(IP)是一种X连锁显性疾病,临床表现极为多样。诊断不明确会使遗传咨询以及在Xq28中精确定位该基因的工作变得复杂。X染色体失活模式的明显偏斜是色素失禁症的一个标志,为研究不确定病例提供了一种方法。我们对三个家庭进行了X染色体失活研究,在这些家庭中,Xq28标记研究结果与最初的临床评估不一致。结果表明,疾病基因座和Xq28基因座之间未发生重组,并提示嵌合体是导致其中一个家庭出现差异的原因。