Further evidence from two families that craniofrontonasal dysplasia maps to Xp22

被引:6
作者
Pulleyn, LJ
Winter, RM
Reardon, W
McKeown, C
Jones, B
Hayward, R
Evans, R
Malcolm, S
机构
[1] UCL, Inst Child Hlth, Mol Genet Unit, London WC1N 1EH, England
[2] UCL, Inst Child Hlth, Mothercare Unit Clin Genet & Fetal Med, London WC1N 1EH, England
[3] Great Ormond St Hosp Sick Children, Cranofacial Unit, London WC1N 3JH, England
[4] Birmingham Womens Hosp, Clin Genet Unit, Birmingham, W Midlands, England
关键词
craniofrontonasal dysplasia; haplotype analysis; mild phenotype; Xp22;
D O I
10.1034/j.1399-0004.1999.550613.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Craniofrontonasal dysplasia (CFND) is a rare X-linked disorder that maps to a 13-cM region on Xp22. Phenotypic features include craniosynostosis, hypertelorism and a broad nasal root with or without a bifid nasal tip. Multiple examples have been reported of males having a less severe phenotype than females. We report haplotype analyses in two CFND families over the critical region to which the gene has been mapped. In pedigree 1, a clinically unaffected male inherited the affected marker haplotype spanning the critical region. We suggest that this individual does have the CFND mutation, but has an extremely mild phenotype that is not detectable with clinical examination. Under the assumption that he is an unknown phenotype, a combined two-point LOD score of 1.68 at zero recombination was obtained, increasing the previously reported total to 5.61 (DXS8022). The data do not narrow down the critical region. This result stresses the importance of subjecting fathers of apparently sporadic cases to a highly critical medical examination and may also explain the unequal ratio of reported female-to-male cases.
引用
收藏
页码:473 / 477
页数:5
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