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Developmental Syndromes and Malformations of the Urinary Tract

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Pediatric Nephrology

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Abstract

Birth defects involving the kidney and urinary system are often encountered and frequently occur in association with other structural abnormalities. A congenital urinary tract anomaly may provide the first clue to the recognition of multiorgan developmental abnormalities. Nevertheless many renal anomalies remain asymptomatic and undiagnosed. Therefore it is critical, not only for pediatric nephrologists but also for pediatricians in general, to be familiar with the common anomalies involving the kidney and urinary system and the more complex disorders with which they may be associated.

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Authors and Affiliations

  1. Department of Medicine, Division of Medical Genetics, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkoknoi, Bangkok, Thailand

    Chanin Limwongse

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  1. Chanin Limwongse
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Correspondence to Chanin Limwongse .

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Editors and Affiliations

  1. Department of Pediatrics, Medical College of Wisconsin, Children’s Research Institute, Children’s Hospital, Health System of Wisconsin, Milwaukee, Wisconsin, USA

    Ellis D. Avner

  2. Boston Children’s Hospital, Harvard Medical School, Boston, Massachusetts, USA

    William E. Harmon

  3. Service de Néphrologie Pédiatrique, Hôpital Necker-Enfants Malades, Université Paris-Descartes, Paris, France

    Patrick Niaudet

  4. Department of Pediatrics, Wakayama Medical University, Wakayama City, Japan

    Norishige Yoshikawa

  5. Division of Nephrology, Bambino Gesù Children’s Hospital – IRCCS, Rome, Italy

    Francesco Emma

  6. Division of Nephrology and Hypertension, The Heart Institute, Cincinnati Children’s Hospital Medical Center, College of Medicine, Cincinnati, Ohio, USA

    Stuart L. Goldstein

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Limwongse, C. (2016). Developmental Syndromes and Malformations of the Urinary Tract. In: Avner, E., Harmon, W., Niaudet, P., Yoshikawa, N., Emma, F., Goldstein, S. (eds) Pediatric Nephrology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-43596-0_5

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  • DOI: https://doi.org/10.1007/978-3-662-43596-0_5

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