Ballew C, Beckerman S J, Lizarralde R
Center for Clinical Research, Chicago, IL 60607.
Cleft Palate Craniofac J. 1993 Jul;30(4):411-3. doi: 10.1597/1545-1569_1993_030_0411_hpocla_2.3.co_2.
Cleft lip with or without cleft palate (CL +/- P) is of high prevalence in an isolated, inbred indigenous population of the Venezuelan rain forest: 12 contemporary probands are known in a population of 1200. CL +/- P is familial in this population. One kindred contains four affected siblings and a total of eight probands. The mode of transmission of CL +/- P is under investigation through the collection and biological verification of genealogies and through screening for selected sequence-based polymorphisms. Polymerase chain reaction (PCR) assays were successfully applied to recover DNA from blood dried onto filter paper in the field. Eleven samples from probands and their first-degree relatives have been analyzed for DNA sequence-based polymorphisms for TGF-A and HOX7. No significant linkages for either locus were found. Evaluation of the distribution of probands in four genealogies indicates that CL +/- P could be transmitted as an autosomal recessive trait in this population. We believe this is the first report of this mode of transmission for nonsyndromic CL +/- P.
在委内瑞拉雨林中一个与世隔绝、近亲通婚的原住民群体中,唇裂伴或不伴腭裂(CL +/- P)的发病率很高:在1200人的群体中有12名当代先证者。在这个群体中,CL +/- P具有家族性。一个家族中有四个受影响的兄弟姐妹,共有八个先证者。目前正在通过收集和生物学验证系谱以及筛选选定的基于序列的多态性来研究CL +/- P的遗传模式。聚合酶链反应(PCR)检测已成功应用于从野外滤纸上干燥的血液中提取DNA。已对来自先证者及其一级亲属的11个样本进行了TGF-A和HOX7基于DNA序列的多态性分析。未发现任何一个基因座有显著连锁。对四个系谱中先证者分布的评估表明,CL +/- P在该群体中可能作为常染色体隐性性状遗传。我们认为这是关于非综合征性CL +/- P这种遗传模式的首次报道。