Sander A, Schmelzle R, Murray J
Clinic of Oral-Maxillofacial Surgery, Nordwestdeutsche Kieferklinik, University of Hambrug, Germany.
Hum Mol Genet. 1994 Apr;3(4):575-8. doi: 10.1093/hmg/3.4.575.
Van der Woude syndrome (VWS) is an autosomal dominant craniofacial disorder representing the most frequent form of syndromic cleft lip and palate. Other characteristic features are pits of the lower lip and hypodontia. The gene shows high penetrance and seems to play an important role in orofacial development determined by the tissues involved and their formation during different periods of craniofacial development. Although most individuals affected with VWS show Mendelian inheritance, one patient with a macroscopic deletion and multiple malformations including two primary features of VWS has been described in the literature, indicating hemizygosity is compatible with the VWS phenotype. We report here the allelic loss of a stable and highly polymorphic microsatellite (D1S205) from region 1q32-41 in one family with VWS. Classical manifestations of the syndrome superimposed on developmental delay in all affected members of the family, the absence of cytogenetic abnormalities, the reproducibility of the null allele with a new set of primers and close linkage of this marker in a total of 15 VWS families provide strong evidence that the first microdeletion involving the gene for VWS has been identified. Assuming 1 Mb of DNA per cM of genetic distance, the upper bound of the deletion size would amount to 4 Mb.
范德伍德综合征(VWS)是一种常染色体显性遗传的颅面疾病,是综合征性唇腭裂最常见的形式。其他特征包括下唇凹陷和牙齿发育不全。该基因具有高外显率,似乎在由颅面发育不同时期所涉及的组织及其形成所决定的口面部发育中起重要作用。尽管大多数VWS患者表现出孟德尔遗传,但文献中描述了一名患有宏观缺失和多种畸形(包括VWS的两个主要特征)的患者,这表明半合子状态与VWS表型相符。我们在此报告一个VWS家族中位于1q32 - 41区域的一个稳定且高度多态的微卫星(D1S205)的等位基因缺失情况。该综合征的典型表现叠加在家族中所有受影响成员的发育迟缓上,无细胞遗传学异常,用一组新引物检测到的无效等位基因的可重复性以及该标记在总共15个VWS家族中的紧密连锁,提供了有力证据表明已鉴定出首例涉及VWS基因的微缺失。假设每厘摩遗传距离对应1兆碱基对的DNA,缺失大小的上限将达4兆碱基对。