Original Article
Subject Category: Genetics
Journal of Investigative Dermatology (2006) 126, 300–304. doi:10.1038/sj.jid.5700103; published online 29 December 2005
The Gene for a Rare Autosomal Dominant Form of Pompholyx Maps to Chromosome 18q22.1–18q22.3
Jian-Jun Chen1,2,4, Yan-Hua Liang1,2,4, Fu-Sheng Zhou2, Sen Yang1,2, Jian Wang1,2, Pei-Guang Wang1,2, Wen-Hui Du1,2, Shi-Jie Xu3, Wei Huang3 and Xue-Jun Zhang1,2
- 1Department of Dermatology at First Hospital, Institute of Dermatology, Anhui Medical University, Hefei, Anhui, China
- 2Key Laboratory of Genome Research at Anhui, Hefei, Anhui, China
- 3Chinese National Human Genome Center at Shanghai, Shanghai, China
Correspondence: Dr Wei Huang, Chinese National Human Genome Center at Shanghai, 250 Bi Bo Road, Shanghai 201203, PR China. E-mail: Huangwei@chgc.sh.cn; Professor Xue-Jun Zhang, Institute of Dermatology, Anhui Medical University, 69 Meishan Road, Hefei, Anhui 230032, China. E-mail: ayzxj@vip.sina.com
4These authors contributed equally to this work
Received 24 September 2005; Revised 24 September 2005; Accepted 16 October 2005; Published online 29 December 2005.
Abstract
Pompholyx is a rather common disorder characterized by recurrent crops of vesicles or bullae on the lateral aspects of the fingers, as well as the palms and soles with non-erythematous skin. Until now, very few large families have been reported, so no gene or locus has been identified. Here, we performed a genome-wide search in a large Chinese family to map the chromosome location of the responsible gene. We identified a locus at chromosome 18q22.1–18q22.3 with a maximum two-point LOD score of 3.61 at marker D18S1131 (
=0.00). Haplotype analyses indicated that the disease gene is located within 12.07 cM region between markers D18S465 and D18S1362, which corresponds to 8.0 Mb. This is the first locus identified for pompholyx. It will aid future identification of the responsible gene, which will be useful for the understanding of the molecular mechanism of pompholyx.
Abbreviations:
OMIM, Online Mendelian Inheritance in Man
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