Donnai D, Read A P, McKeown C, Andrews T
Regional Genetics Service, St. Mary's Hospital, Manchester.
J Med Genet. 1988 Dec;25(12):809-18. doi: 10.1136/jmg.25.12.809.
We describe three patients with the cutaneous manifestations of hypomelanosis of Ito. Two, with unusual abnormalities of their toes, had a mixture of diploid and triploid cells in cultured skin fibroblasts. The published clinical descriptions of hypomelanosis of Ito and diploid-triploid mosaicism are reviewed. Chromosome heteromorphisms, HLA types, and DNA fingerprints were studied in an attempt to elucidate the origin of the disease in our patients. We conclude that hypomelanosis of Ito is a manifestation of a heterogeneous group of disorders, the common factor being the presence of two genetically different cell lines. It can result from chromosomal mosaicism or chimerism, from a postzygotic mutation, or from X inactivation. The risk of recurrence is negligible if the proband is a male; if the proband is female the risk is also low but an X linked mutation must be considered.
我们描述了3例具有伊藤色素减退皮肤表现的患者。其中2例脚趾有异常,其培养的皮肤成纤维细胞中存在二倍体和三倍体细胞的混合。本文回顾了已发表的伊藤色素减退和二倍体 - 三倍体嵌合体的临床描述。为了阐明我们患者中疾病的起源,研究了染色体异态性、HLA类型和DNA指纹。我们得出结论,伊藤色素减退是一组异质性疾病的表现,共同因素是存在两种基因不同的细胞系。它可能由染色体嵌合体或嵌合现象、合子后突变或X染色体失活引起。如果先证者是男性,复发风险可忽略不计;如果先证者是女性,风险也较低,但必须考虑X连锁突变。