Mutational analysis of SHH and GLI3 in anorectal malformations.
作者信息
Garcia-Barceló Maria-Mercè, Chi-Hang Lui Vincent, Miao Xiaoping, So Man-ting, Yuk-yu Leon Thomas, Yuan Zhen-wei, Li Long, Liu Lei, Wang Bin, Sun Xiao-bing, Huang Liu-Ming, Tou Jin-fa, Sau-wai Ngan Elly, Cherny Stacey S, Chan Kin-wai, Lee Kim-hung, Wang Weiling, Kak-yuen Wong Kenneth, Kwong-hang Tam Paul
机构信息
Department of Surgery, University of Hong Kong, Hong Kong SAR, China.
出版信息
Birth Defects Res A Clin Mol Teratol. 2008 Sep;82(9):644-8. doi: 10.1002/bdra.20482.
BACKGROUND
Anorectal malformations (congenital absence of the anal opening) are among the most common pediatric surgical problems and carry a significant chronic morbidity.
METHODS
Direct sequencing was used to screen 88 anorectal malformations patients for mutations and polymorphisms in SHH and GLI3. These genes were chosen according to the phenotype presented by mutant mice and their expression patterns.
RESULTS
We report on 10 GLI3 variants (IVS3+141C>G, T183A, IVS4+124T>C, IVS7+17G>A, IVS8+1 G>C, N503N, P941P, P998L, A1005A, A1039A) and four SHH mutation/variants (IVS1-49C>T, IVS2+111A>C, L214L, G290D).
CONCLUSIONS
These variants are not over-represented in the healthy population and most are predicted to be benign. This study conveys the problematic assessment of the pathogenic role in disease of rare point mutations and variants.
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