From
Dr. Marc Levitt
Fetal and Newborn Management of Cloacal Malformations
pubmed.ncbi.nlm.nih.gov shows its articles on its own site.
Read the article on pubmed.ncbi.nlm.nih.gov ↗Article · Jul 2026 · 1 min read
In brief
In brief
This article addresses the prenatal detection and postnatal management of cloacal malformations, rare congenital anomalies where the genitourinary and anorectal tracts share a single perineal opening in females. It covers diagnostic approaches, associated anomalies, and surgical management strategies for this complex condition.
Written by the GCMD Library team from the article.
Cloaca is a rare, complex malformation encompassing the genitourinary and anorectal tract of the female in which these tracts fail to separate in utero, resulting in a single perineal orifice. Prenatal sonography detects a few cases with findings such as renal and urinary tract malformations, intral …
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Transanal-only Swenson-like pull-through for late diagnosed Hirschsprung disease
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Corrigendum: Sacral Curvature in Addition to Sacral Ratio to Assess Sacral Development and the Association With the Type of Anorectal Malformations
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Validation of a Newly Developed Competency Assessment Tool for the Posterior Sagittal Anorectoplasty
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Antegrade Continence Enema Alone for the Management of Functional Constipation and Segmental Colonic Dysmotility (ACE-FC): A Pediatric Colorectal and Pelvic Learning Consortium Study
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More evidence against appendectomy at the time of a Ladd procedure
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