| Persistent Cloaca
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Etiology
Unknown.
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Pathogenesis
The abnormality results from failure of the urorectal septum to separate the primitive urogenital sinus from the hindgut.,
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Epidemiology
Developmental disorder detected prenatally or at birth.
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General Gross Description
The diagnosis rests on the gross demonstration of a common structure serving as bladder and rectum.
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General Microscopic Description
Not applicable.
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Clinical Correlation
Associated anomalies may include imperforate anus, abscence of genital and urinary orifices, megacolon, megaureters, renal dysplasia, renal agenesis.
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References
Textbook of Fetal and Perinatal Pathology. Wigglesworth JS and Singer DB (eds) Cambridge: Blackwell, 1989, pp. 1163-4. Langman's Medical Embryology, 6th edition. 1990. Sadler TW. Baltimore: Williams and Wilkins. pp. 75, 255, 268.
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| Persistent Cloaca
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| Synopsis by: Harold Yamase M.D. (T74000M20000)[480]
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