Literature DB >> 26791133

Cloacal dysgenesis sequence with bilateral renal agenesis and normal pulmonary development in twin pregnancy.

Sundram Jegadeesh1, Jai Kumar Mahajan1.   

Abstract

Cloacal dysgenesis sequence (CDS) is a rare congenital anomaly. It is characterised by a smooth perineum with absence of anal and genitourinary orifices, with reported incidence of 1:50,000-250,000 births. Association with bilateral renal agenesis is still rarer and resultant severe oligohydramnios is associated with pulmonary hypoplasia. Only a few cases of CDS with bilateral renal agenesis have been reported in the English language literature, with associated pulmonary hypoplasia as a default phenomenon. We report a case of CDS and bilateral renal agenesis without associated pulmonary hypoplasia in a twin pregnancy, which, to the best of our knowledge, is the second reported case of this amalgamation. 2016 BMJ Publishing Group Ltd.

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Year:  2016        PMID: 26791133      PMCID: PMC4735355          DOI: 10.1136/bcr-2015-214130

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  16 in total

1.  Long-term survival with cloacal dysgenesis sequence.

Authors:  Toshihiro Yanai; Yasuhisa Urita; Teruyoshi Amagai; Hajime Kawakami; Hiroko Watayo; Takayuki Masuko; Satoshi Matsuda; Misako Hirai; Toshihiro Muraji; Hiromi Hamada
Journal:  Pediatr Surg Int       Date:  2012-01       Impact factor: 1.827

Review 2.  Is urorectal septum malformation sequence a variant of the vertebral defects, anal atresia, tracheo-oesophageal fistula, renal defects and radial dysplasia association? Report of a case and a review of the literature.

Authors:  Jen-Chung Chien; Shu-Jen Chen; Chui-Mei Tiu; Yann-Jang Chen; Betau Hwang; Dau-Ming Niu
Journal:  Eur J Pediatr       Date:  2005-02-24       Impact factor: 3.183

3.  Caudal mesoderm pattern of anomalies: from renal agenesis to sirenomelia.

Authors:  B Källén; J Winberg
Journal:  Teratology       Date:  1974-02

4.  Fetal breathing movements as predictor of favourable pregnancy outcome after oligohydramnios due to membrane rupture in second trimester.

Authors:  M Blott; A Greenough; K H Nicolaides; G Moscoso; D Gibb; S Campbell
Journal:  Lancet       Date:  1987-07-18       Impact factor: 79.321

5.  A syndrome of multiple congenital malformations with absent external genitalia, urethral and anal openings in one of twins.

Authors:  D Sinniah; J K Manuel
Journal:  Singapore Med J       Date:  1980-04       Impact factor: 1.858

6.  Agenesis of the penis, scrotal raphe, and anus in one of monoamniotic twins.

Authors:  S A Berry; D E Johnson; T R Thompson
Journal:  Teratology       Date:  1984-04

7.  Persistent cloaca with absent penis and anal atresia in one of identical twins.

Authors:  H Koffler; J M Aase; L A Papile; R W Coen
Journal:  J Pediatr       Date:  1978-11       Impact factor: 4.406

8.  Long-term survival and renal transplantation in a monozygotic twin with cloacal dysgenesis sequence.

Authors:  Rita A Mukhtar; Laurence S Baskin; Peter G Stock; Hanmin Lee
Journal:  J Pediatr Surg       Date:  2009-12       Impact factor: 2.545

9.  Urorectal septum malformation sequence: a report of seven cases.

Authors:  Deepali Jain; Mehar C Sharma; Kalyani K Kulkarni; Shipra Aggrawal; Asis K Karak
Journal:  Congenit Anom (Kyoto)       Date:  2008-12       Impact factor: 1.409

10.  The prenatal diagnosis of cloacal dysgenesis sequence in six cases: can the termination of pregnancy always be the first choice?

Authors:  Zeki Sahinoglu; Baris Mulayim; Selcuk Ozden; Seref Etker; Aysenur Celayir; Ferda Ozkan; Remziye Bilgic
Journal:  Prenat Diagn       Date:  2004-01       Impact factor: 3.050

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