Ikeda S, Wakem P, Haake A, Ewing N, Polakowska R, Sarret Y, Trattner A, David M, Shohat M, Schroeder D W
Department of Dermatology, University of California, San Francisco.
J Invest Dermatol. 1994 Oct;103(4):478-81. doi: 10.1111/1523-1747.ep12395577.
Darier disease is an autosomal dominant abnormality of epidermal differentiation characterized clinically by the presence of hyperkeratotic papules on the skin and histologically by the loss of cell cohesion and by disorderly keratinization. Two groups recently found evidence that the gene whose mutations underlie this disease is located at chromosome 12q23-q24.1, a site on chromosome 12 that clearly is distal to the type II keratin gene cluster. We report here evidence for sublocalization to a 5-cM region of that site in an additional ten families of European and Middle Eastern ancestry with a combined lod score in excess of 20.
毛囊角化病是一种常染色体显性遗传性表皮分化异常疾病,临床特征为皮肤上出现角化过度丘疹,组织学特征为细胞间黏附丧失和角化紊乱。最近有两个研究小组发现,该疾病相关基因突变所在的基因位于12号染色体的q23 - q24.1区域,该区域明显位于II型角蛋白基因簇的远端。我们在此报告,在另外10个欧洲和中东血统的家族中,有证据表明该疾病相关基因亚定位在该位点的一个5厘摩区域,其合并对数优势得分超过20。