Literature DB >> 16610483

Cloacal exstrophy.

Susanne Jane Hyun1.   

Abstract

Cloacal exstrophy is an extremely rare and devastating complex of congenital abnormalities resulting in multiple debilitating morbidities. Infants with this disorder require numerous surgical interventions to repair gastrointestinal, genitourinary, spinal, and orthopedic malformations. Treatment involves the combined efforts of many medical and nursing specialists. This article discusses the embryology, clinical presentation, and management (both early and long term) of cloacal exstrophy, with emphasis on gender reassignment issues and quality of life.

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Year:  2006        PMID: 16610483     DOI: 10.1891/0730-0832.25.2.101

Source DB:  PubMed          Journal:  Neonatal Netw        ISSN: 0730-0832


  3 in total

1.  Fetal MRI of cloacal exstrophy.

Authors:  Maria A Calvo-Garcia; Beth M Kline-Fath; Eva I Rubio; Arnold C Merrow; Carolina V Guimaraes; Foong-Yen Lim
Journal:  Pediatr Radiol       Date:  2012-11-27

2.  A rare presentation of OEIS variant with a recto-bladder neck fistula: A case report and literature review.

Authors:  Athari AlShammari; Waleed Burhamah; Amar Alnaqi
Journal:  Int J Surg Case Rep       Date:  2022-05-04

3.  A case of congenital cloacal exstrophy/omphalocele-exstrophy-imperforate anus-spinal defects syndrome and a successful pregnancy.

Authors:  Mara Seat; Munira Boxwalla; Arielle Hough; Glenn Goodwin
Journal:  Clin Exp Reprod Med       Date:  2022-09-01
  3 in total

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