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Variable expression of Van der Woude syndrome: A case report
Author(s) -
Altuntaş Zeynep,
Ismayilzade Majid,
Altuntaş Mahmut,
Yildirim Mehmet E. C.
Publication year - 2020
Publication title -
surgical practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.109
H-Index - 10
eISSN - 1744-1633
pISSN - 1744-1625
DOI - 10.1111/1744-1633.12459
Subject(s) - medicine , variable expression , dermatology , genetics , biology , gene
Van der Woude syndrome (VWS) is an autosomal dominant disorder with a rare clinical manifestation of orofacial disorders with deletion in the 1q32‐q41 chromosome band. In our study we present a clinical case of a 1‐year old boy with a bilateral cleft lip, a cleft palate and bilateral congenital pits on the lower lip and a father with various clinical presentations of VWS.
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