Literature DB >> 7395906

The van der Woude syndrome in a large kindred: variability, penetrance, genetic risks.

P Janku, M Robinow, T Kelly, R Bralley, A Baynes, M T Edgerton.   

Abstract

The van der Woude syndrome was studied in a seven-generation kindred. Lip pits were the most common manifestation of affected persons. They occurred in 88% of the affected and were the only manifestations in 64%; clefts of lip and palate occurred in 21%. Penetrance was 96.7%. Careful examination showed minor manifestations of the syndrome in several individuals who had considered themselves unaffected. The distribution of manifestations and the risk to off-spring differed appreciably from that reported in the literature. The implications of these findings for genetic counseling are discussed.

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Mesh:

Year:  1980        PMID: 7395906     DOI: 10.1002/ajmg.1320050203

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  16 in total

Review 1.  Developmental disorders of the dentition: an update.

Authors:  Ophir D Klein; Snehlata Oberoi; Ann Huysseune; Maria Hovorakova; Miroslav Peterka; Renata Peterkova
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

2.  Van der Woude Syndrome: IRF6 Mutations.

Authors:  Ansa P Sunny; Gautham Arunachal; Sumita Danda
Journal:  Indian J Pediatr       Date:  2019-08-29       Impact factor: 1.967

3.  A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41.

Authors:  B C Schutte; B C Bjork; K B Coppage; M I Malik; S G Gregory; D J Scott; L M Brentzell; Y Watanabe; M J Dixon; J C Murray
Journal:  Genome Res       Date:  2000-01       Impact factor: 9.043

4.  Surgical, Speech, and Audiologic Outcomes in Patients With Orofacial Cleft and Van der Woude Syndrome.

Authors:  Spencer Kitchin; Lynn Grames; Sybill D Naidoo; Gary Skolnick; Alyssa Schoenborn; Alison Snyder-Warwick; Kamlesh Patel
Journal:  J Craniofac Surg       Date:  2019-07       Impact factor: 1.046

5.  Linkage studies in a pedigree with Van der Woude syndrome.

Authors:  T F Wienker; G Hudek; S Bissbort; A Mayerová; G Mauff; K Bender
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

6.  Linkage analysis in a large Brazilian family with van der Woude syndrome suggests the existence of a susceptibility locus for cleft palate at 17p11.2-11.1.

Authors:  A L Sertié; A V Sousa; S Steman; R C Pavanello; M R Passos-Bueno
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

Review 7.  Toward an orofacial gene regulatory network.

Authors:  Youssef A Kousa; Brian C Schutte
Journal:  Dev Dyn       Date:  2015-09-17       Impact factor: 3.780

8.  Linkage of Van der Woude syndrome (VWS) to REN and exclusion of the candidate gene TGFB2 from the disease locus in a large pedigree.

Authors:  A Sander; H Moser; S Liechti-Gallati; T Grimm; M Zingg; J Raveh
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

9.  Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletion.

Authors:  Shuji Kayano; Shigeo Kure; Yoichi Suzuki; Kiyoshi Kanno; Yoko Aoki; Shinji Kondo; Brian C Schutte; Jeffrey C Murray; Atsushi Yamada; Yoichi Matsubara
Journal:  J Hum Genet       Date:  2003-11-15       Impact factor: 3.172

10.  Novel mutations mapping to the fourth sodium channel domain of Nav1.7 result in variable clinical manifestations of primary erythromelalgia.

Authors:  Roman Cregg; Bisola Laguda; Robert Werdehausen; James J Cox; John E Linley; Juan D Ramirez; Istvan Bodi; Michael Markiewicz; Kevin J Howell; Ya-Chun Chen; Karen Agnew; Henry Houlden; Michael P Lunn; David L H Bennett; John N Wood; Maria Kinali
Journal:  Neuromolecular Med       Date:  2013-01-06       Impact factor: 3.843

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