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Van der Woude syndrome: A review of 11 cases seen at the Lagos University Teaching Hospital

Title: Van der Woude syndrome: A review of 11 cases seen at the Lagos University Teaching Hospital
Authors: James, O; Adeyemo, WL; Emeka, CI; Ogunlewe, MO; Ladeinde, AL; Butali, A
Source: African Journal of Paediatric Surgery; Vol 11, No 1 (2014); 52-55 ; 0189-6725
Publisher Information: Medknow Publications (India)
Publication Year: 2014
Subject Terms: Cleft lip; cleft palate; lip pits; Van der Woude syndrome; psy; hist
Description: Background: Van der Woude syndrome (VWS), an autosomal dominant condition associated with clefts of the lip and/or palate and lower lip pits and is caused by mutations in interferon regulatory factor six gene. It isreported to be the most common syndromic cleft worldwide. Non-penetrance for the lip pit phenotype is found in at least 10% of affected individuals and those without the pits are phenocopies for non-syndromic clefting. The aim of this study is to present the phenotypiccharacteristic of VWS seen at the Lagos University Teaching Hospital (LUTH) cleft clinic.Materials and Methods: A review of cases of patients with VWS that attended the cleft lip and palate clinic at the LUTH Idi-Araba, Lagos, from January 2007 to December 2012 was conducted. Data analyses included sex of affected patients, types of cleft, presence of lower lip pits andhistory of lower lip pits/cleft in the family.Results: A total of 11 cases were seen during the period (male = 4; female = 7). Age at presentation ranged between 1 week and 12 years, with majority (n = 10) less than 2 years of age. Bilateral cleft lip and palate (BCLP) was seen in six patients, isolated soft palatal cleft (n = 3)and unilateral cleft lip and alveolus (n = 1) and cleft of hard and soft palate (n = 1). Bilateral lower lips were presented in 10 out of the 11 cases. The mother of the only patient without lip pits presented with bilateral lower lip pits. No family history of cleft/lip pits was elicited in 10 other cases. Conclusion: Most of the cases of VWS presented with BCLP and lower lippits. Non-penetrance for the lip pits was seen in one out of 11 cases. Our study emphasizes the need to screen family members in all cleft cases, especially clinically diagnosed non-syndromic cases who may be VWS with no lip pits. Future studies are required to investigate the genetic causes of this syndrome in our population.Key words: Cleft lip, cleft palate, lip pits, Van der Woude syndrome
Document Type: article in journal/newspaper
Language: English
Relation: http://www.ajol.info/index.php/ajps-n/article/view/103104
Availability: http://www.ajol.info/index.php/ajps-n/article/view/103104
Rights: undefined
Accession Number: edsbas.2FEA1032
Database: BASE