| Literature DB >> 31488442 |
Dilharan D Eliezer1,2, Himanshu Goel2,3, Virginia M Turner4, Aniruddh Deshpande1,2,5.
Abstract
Van der Woude syndrome (VWS) and popliteal pterygium syndrome (PPS) spectrum are due to genetic variants in the IRF6 which phenotypically has been known to manifest with midline defects such as cleft lip and palate in VWS and additional nail, limb and genital anomalies in PPS. We report a case of VWS with the previously unrecognised phenotypic feature of hemiscrotal agenesis. While bifid scrotum has been reported in the more severe PPS, neither VWS nor PPS have previously noted hemiscrotal agenesis as part of the phenotypic picture. Hemiscrotal agenesis without evidence of any genetic anomaly has only been reported four times in the literature to date with two of these being accompanied by complete testicular descent. Treatment options include topical androgen application and/or scrotoplasty to allow for adequate testicular thermoregulation and development to occur. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: genetics; infant health; paediatric surgery; plastic and reconstructive surgery; urological surgery
Mesh:
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Year: 2019 PMID: 31488442 PMCID: PMC6731811 DOI: 10.1136/bcr-2019-229938
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X