Literature DB >> 25478421

A case of vander woude syndrome with rare phenotypic expressions.

Anurag Tripathi1, Brijesh Tiwari2, Shalini Gupta3, Ranjit Patil4, Vikram Khanna5.   

Abstract

Van der Woude syndrome (VWS) is a rare developmental disorder with an autosomal dominant inheritance. The prevalence of VWS varies from 1:100,000 to 1:40,000 still born or live births. It has variable expressivity and generally expressed as orofacial manifestations like lower lip pits, cleft lip and/or cleft palate, hypodontia, cleft or bifid uvula, ankyloglossia and some extraoral anomalies involving hand, foot and genitalia. Thorough family history, clinical examination and genetic counseling helps in correct diagnosis of VWS as Popliteal pterygium syndrome has overlapping clinical manifestations. Most cases of Van der Woude syndrome have been associated with mutations and genetic changes. The current case has classical features of VWS with some rare features like undescended small testis and unreported finding of syndactyly of second and third toe adds on to the existing knowledge of VWS presentation.

Entities:  

Keywords:  Lip pits; Popliteal pterygium syndrome; Syndactyly; Van der woude syndrome

Year:  2014        PMID: 25478421      PMCID: PMC4253239          DOI: 10.7860/JCDR/2014/10420.5008

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  12 in total

1.  Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32.

Authors:  M M Lees; R M Winter; S Malcolm; H M Saal; L Chitty
Journal:  J Med Genet       Date:  1999-12       Impact factor: 6.318

2.  Phenotypic variation in the popliteal pterygium syndrome.

Authors:  D Bixler; C Poland; W E Nance
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

3.  Normative values for testicular volume measured by ultrasonography in a normal population from infancy to adolescence.

Authors:  J Goede; W W M Hack; K Sijstermans; L M van der Voort-Doedens; T Van der Ploeg; A Meij-de Vries; H A Delemarre-van de Waal
Journal:  Horm Res Paediatr       Date:  2011-04-05       Impact factor: 2.852

4.  Cleft lip and palate, lower lip pits, and limb deficiency defects.

Authors:  W Küster; J T Lambrecht
Journal:  J Med Genet       Date:  1988-08       Impact factor: 6.318

5.  Clinical and genetic features of Van der Woude syndrome in two large families in Brazil.

Authors:  Hercílio Martelli-Junior; Marcelo Reis Chaves; Mário Sérgio Oliveira Swerts; Roseli Teixeira de Miranda; Paulo Rogério Ferreti Bonan; Ricardo D Coletta
Journal:  Cleft Palate Craniofac J       Date:  2007-05

6.  The Van der Woude syndrome (dominantly inherited lip pits and clefts).

Authors:  A Schinzel; M Kläusler
Journal:  J Med Genet       Date:  1986-08       Impact factor: 6.318

7.  Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.

Authors:  Myriam Peyrard-Janvid; Elizabeth J Leslie; Youssef A Kousa; Tiffany L Smith; Martine Dunnwald; Måns Magnusson; Brian A Lentz; Per Unneberg; Ingegerd Fransson; Hannele K Koillinen; Jorma Rautio; Marie Pegelow; Agneta Karsten; Lina Basel-Vanagaite; William Gordon; Bogi Andersen; Thomas Svensson; Jeffrey C Murray; Robert A Cornell; Juha Kere; Brian C Schutte
Journal:  Am J Hum Genet       Date:  2013-12-19       Impact factor: 11.025

8.  Congenital bilateral lower lip pits associated with fistulae of the minor salivary glands: case report of the principal Van der Woude syndrome's trait.

Authors:  Luís Ricardo Martinhão Souto
Journal:  Aesthetic Plast Surg       Date:  2008-01       Impact factor: 2.326

9.  Van der Woude syndrome: clinical presentation in 64 patients.

Authors:  Jung-Ju Huang; Jia-Woei Hou; Ying-Chien Tan; Kuo-Ting Chen; Lun-Jou Lo; Yu-Ray Chen
Journal:  Cleft Palate Craniofac J       Date:  2007-11

Review 10.  Van der Woude syndrome: a review. Cardinal signs, epidemiology, associated features, differential diagnosis, expressivity, genetic counselling and treatment.

Authors:  Maria Rizos; Meropi N Spyropoulos
Journal:  Eur J Orthod       Date:  2004-02       Impact factor: 3.075

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