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Rare Congenital Genitourinary Anomalies : An Illustrated Reference Guide / by Mohamed A Baky Fahmy

By: Fahmy, Mohamed A. Baky
Material type: materialTypeLabelE-bookPublisher: Berlin, Heidelberg : Springer, 2015Description: 1 recurso en línea (XVI, 235 p.) 346 il., 283 il. col..ISBN: 9783662436806.Subject: Aparato urinario -- EnfermedadesDDC classification: 617 Online resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources Summary: Patients with rare diseases, affecting less than 1 in 2000 persons, frequently experience delays or errors in diagnosis, sometimes with tragic consequences. Even after the diagnosis has been established, the quality of health care delivered is often poor. This book, which is both textbook and atlas, covers the full range of rare congenital genitourinary anomalies encountered in males and females, many of which have previously been described only in sporadic case reports. In the case of the more established anomalies, variants are presented. For each anomaly, information is provided on incidence, similar cases, clinical presentation, diagnosis, possible management and outcome. Informative supporting illustrations are presented for each anomaly, and the book will serve as an excellent reference for all pediatricians, urologists and surgeons who are responsible for the care of such patients.
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Holdings
Item type Current library Collection Call number Copy number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud RC872 .F346 2015 EB (Browse shelf(Opens below)) .i11579377 Acceso electrónico eBOOK .i11579377
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Patients with rare diseases, affecting less than 1 in 2000 persons, frequently experience delays or errors in diagnosis, sometimes with tragic consequences. Even after the diagnosis has been established, the quality of health care delivered is often poor. This book, which is both textbook and atlas, covers the full range of rare congenital genitourinary anomalies encountered in males and females, many of which have previously been described only in sporadic case reports. In the case of the more established anomalies, variants are presented. For each anomaly, information is provided on incidence, similar cases, clinical presentation, diagnosis, possible management and outcome. Informative supporting illustrations are presented for each anomaly, and the book will serve as an excellent reference for all pediatricians, urologists and surgeons who are responsible for the care of such patients.

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