Meeting report on the NIDDK/AUA Workshop on Congenital Anomalies of External Genitalia: challenges and opportunities for translational research

H. Scott Stadler, Craig A. Peters, Renea M. Sturm, Linda A. Baker, Carolyn J.M. Best, Victoria Y. Bird, Frank Geller, Deborah K. Hoshizaki, Thomas B. Knudsen, Jenna M. Norton, Rodrigo L.P. Romao, Martin J. Cohn

Research output: Contribution to journalReview articlepeer-review

10 Citations (Scopus)

Abstract

Congenital anomalies of the external genitalia (CAEG) are a prevalent and serious public health concern with lifelong impacts on the urinary function, sexual health, fertility, tumor development, and psychosocial wellbeing of affected individuals. Complications of treatment are frequent, and data reflecting long-term outcomes in adulthood are limited. To identify a path forward to improve treatments and realize the possibility of preventing CAEG, the National Institute of Diabetes and Digestive and Kidney Diseases and the American Urological Association convened researchers from a range of disciplines to coordinate research efforts to fully understand the different etiologies of these common conditions, subsequent variation in clinical phenotypes, and best practices for long term surgical success. Meeting participants concluded that a central data hub for clinical evaluations, including collection of DNA samples from patients and their parents, and short interviews to determine familial penetrance (small pedigrees), would accelerate research in this field. Such a centralized datahub will advance efforts to develop detailed multi-dimensional phenotyping and will enable access to genome sequence analyses and associated metadata to define the genetic bases for these conditions. Inclusion of tissue samples and integration of clinical studies with basic research using human cells and animal models will advance efforts to identify the developmental mechanisms that are disrupted during development and will add cellular and molecular granularity to phenotyping CAEG. While the discussion focuses heavily on hypospadias, this can be seen as a potential template for other conditions in the realm of CAEG, including cryptorchidism or the exstrophy–epispadias complex. Taken together with long-term clinical follow-up, these data could inform surgical choices and improve likelihood for long-term success.

Original languageEnglish
Pages (from-to)791-804
Number of pages14
JournalJournal of Pediatric Urology
Volume16
Issue number6
DOIs
Publication statusPublished - Dec 2020

Bibliographical note

Funding Information:
The authors served as the writing group for the NIDDK/AUA Workshop on Congenital Anomalies of the External Genitalia and gratefully acknowledge the contributions of the following workshop participants: Andrew Adey (Oregon Health and Science University), Darius Bagli (University of Toronto), Larry Baskin (University of California - San Francisco), Spyros Darmanis (Chan Zuckerberg Biohub), L. Earl Gray (U.S. Environmental Protection Agency), Dorrie Lamb (Weill Cornell Medicine), Sean Li (Boston Children's Hospital), Liang Ma (Washington University), Andrew Pask (University of Melbourne), Eric Vilain (Children's National Medical Center and George Washington University), and Duncan Wilcox (University of Texas Southwestern Medical Center).

Publisher Copyright:
© 2020 Journal of Pediatric Urology Company

ASJC Scopus Subject Areas

  • Pediatrics, Perinatology, and Child Health
  • Urology

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