Department of Dermatology, Chang Gung Memorial Hospital, Kaohsiung Medical Center, Chang Gung University, College of Medicine, 123, Ta-pei Road, Kaohsiung Hsien, Taiwan.
Br J Dermatol. 2010 May;162(5):1083-7. doi: 10.1111/j.1365-2133.2010.09677.x. Epub 2010 Feb 3.
The condition of multiple syringomas is a common skin problem that begins in early adulthood and is characterized by the appearance of skin-coloured papules around the eyes. Previous reports have demonstrated that some cases of multiple syringomas are inherited in an autosomal dominant manner.
To identify the genetic factors involved in the development of multiple syringomas.
We recruited seven families including multiple family members with multiple syringomas. Our sample included 24 affected individuals and 11 unaffected individuals. We performed genome-wide single-nucleotide polymorphism screening for linkage analysis.
Whole-genome screening and subsequent analysis revealed that all of the seven families were linked at a locus on chromosome 16q22. A significant logarithm of the odds score of 4.51 with theta of 0.00 confirmed the mapping result. The analysis of critical recombinants defined the locus as a 6.63 cM interval in which 143 genes could be identified.
We confirmed that the condition of multiple syringomas is an autosomal dominant disorder, and we determined the genomic location of the responsible gene.
多发性汗管瘤是一种常见的皮肤问题,通常在成年早期出现,表现为眼周肤色丘疹。先前的报告表明,一些多发性汗管瘤病例呈常染色体显性遗传方式。
鉴定多发性汗管瘤发病的遗传因素。
我们招募了 7 个家族,每个家族都有多发性汗管瘤患者。我们的样本包括 24 名受累个体和 11 名未受累个体。我们对全基因组单核苷酸多态性进行了连锁分析。
全基因组筛查和后续分析显示,7 个家族均在 16q22 染色体上的一个位点连锁。θ为 0.00 的 4.51 的显著对数值支持了图谱结果。对关键重组体的分析将该位点定义为 143 个基因的 6.63 cM 间隔。
我们证实多发性汗管瘤是一种常染色体显性遗传疾病,并确定了致病基因的基因组位置。