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pubmed-article:9869065pubmed:abstractTextPseudoexstrophy or covered exstrophy is a rare exstrophy variant. The authors report a case of covered exstrophy that presented as a newborn with widely separated pubic bones and rectus muscles, a low-set umbilicus, and a subcutaneous bladder. The anal opening was absent, and there was a complex malformation of the external genitalia consisting of a small, laterally displaced penis and a right-sided ectopic hemiscrotum. Micturition and urinary continence were normal. The child also had a high anorectal malformation with a coexistent type IV congenital pouch colon (CPC) malformation. Both kidneys were normal. Preliminary surgery consisted of a divided sigmoid colostomy proximal to the colonic pouch. The literature is reviewed and the embryogenesis of pseudoexstrophy and its associated malformations are discussed.lld:pubmed
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pubmed-article:9869065pubmed:authorpubmed-author:SharmaAAlld:pubmed
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pubmed-article:9869065pubmed:authorpubmed-author:ChadhaRRlld:pubmed
pubmed-article:9869065pubmed:authorpubmed-author:MahajanJ KJKlld:pubmed
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pubmed-article:9869065pubmed:volume33lld:pubmed
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pubmed-article:9869065pubmed:dateRevised2005-11-17lld:pubmed
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pubmed-article:9869065pubmed:year1998lld:pubmed
pubmed-article:9869065pubmed:articleTitlePseudoexstrophy associated with congenital pouch colon.lld:pubmed
pubmed-article:9869065pubmed:affiliationDepartment of Paediatric Surgery, Lady Hardinge Medical College and Kalawati Saran Children's Hospital, New Delhi, India.lld:pubmed
pubmed-article:9869065pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9869065pubmed:publicationTypeCase Reportslld:pubmed