Literature DB >> 16757909

Prenatal diagnosis and therapy of persistent cloaca: a case report.

Mamoru Morikawa1, Takashi Yamada, Kazutoshi Cho, Hideto Yamada, Hisanori Minakami.   

Abstract

Persistent cloaca is a rare abnormality that occurs only in females and is characterized by a direct communication between the gastrointestinal, urinary, and genital structures resulting in a single perineal opening. A case with massive ascites, two cystic structures arising from the fetal pelvis, bilateral hydroureters, calcified meconium, and cardiac anomalies, in which this condition was diagnosed prenatally is presented here. Copyright (c) 2006 S. Karger AG, Basel.

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Year:  2006        PMID: 16757909     DOI: 10.1159/000092463

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  4 in total

1.  Prenatal diagnosis of cloacal malformations.

Authors:  Andrea Bischoff; Marc A Levitt; Foong Yen Lim; Carolina Guimarães; Alberto Peña
Journal:  Pediatr Surg Int       Date:  2010-11       Impact factor: 1.827

2.  Fetal MRI clues to diagnose cloacal malformations.

Authors:  Maria A Calvo-Garcia; Beth M Kline-Fath; Marc A Levitt; Foong-Yen Lim; Leann E Linam; Manish N Patel; Steven Kraus; Timothy M Crombleholme; Alberto Peña
Journal:  Pediatr Radiol       Date:  2011-03-16

3.  Persistent cloaca with fetal ascites: clinical features and perinatal management.

Authors:  Taku Yamamichi; Takaaki Sakai; Mina Yoshida; Keita Takayama; Naoko Uga; Satoshi Umeda; Shohei Maekawa; Noriaki Usui
Journal:  Pediatr Surg Int       Date:  2022-09-02       Impact factor: 2.003

4.  Case report: Antenatal MRI diagnosis of cloacal dysgenesis syndrome.

Authors:  P Gupta; S Kumar; Raju Sharma; A Gadodia
Journal:  Indian J Radiol Imaging       Date:  2010-05
  4 in total

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