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Lower Urinary Tract Anomalies of Urogenital Sinus and Female Genital Anomalies

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Pediatric Uroradiology

Part of the book series: Medical Radiology ((Med Radiol Diagn Imaging))

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Abstract

Congenital anomalies of the female genital tract result from müllerian duct anomalies and/or abnormalities of the urogenital sinus or cloaca. Failure of fusion of the müllerian ducts results in a wide variety of fusion abnormalities of the uterus, cervix, and vagina (Gruenwald 1941). Müllerian duct abnormalities may occur alone or in association with urogenital sinus or cloacal malformations. Persistence of the cloaca is believed to be caused by an abnormal development of the dorsal part of the cloaca and the urorectal septum (Stephens 1983b; Nievelstein et al. 1998). Urogenital sinus malformations occur after the cloaca has been organized into the urogenital sinus and the anus (Williams and Bloomberg 1976). Early and complete assessment of the patients, including radiological and biochemical examinations, is mandatory to provide an optimal basis for treatment that will have a great influence on the quality of the patient’s later life. Due to the close embryologic relationship between the urinary and the genital tract, malformations involving both organ systems are very common. Understanding the development of the urogenital system is necessary to comprehend the full spectrum of congenital anomalies of the female genitalia.

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© 2001 Springer-Verlag Berlin Heidelberg

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Geley, T.E., Gassner, I. (2001). Lower Urinary Tract Anomalies of Urogenital Sinus and Female Genital Anomalies. In: Fotter, R. (eds) Pediatric Uroradiology. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-59428-1_22

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  • DOI: https://doi.org/10.1007/978-3-642-59428-1_22

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-43557-0

  • Online ISBN: 978-3-642-59428-1

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