Literature DB >> 12861546

Currarino triad associated with Hirschsprung's disease.

Nikolaos Baltogiannis1, Georgios Mavridis, Michail Soutis, Dimitrios Keramidas.   

Abstract

The Currarino syndrome is a rare hereditary condition. The major symptom is chronic constipation from early life, and, in more than 80% of the cases, this condition is diagnosed in the first decade. The authors describe an unusual case of a complete Currarino triad associated with Hirschsprung's disease in a 6-year-old girl, presenting persistent constipation and abdominal distension. The patient is free of symptoms after surgical treatment of anorectal malformation and Hirschsprung's disease. The presacral mass was excised. Complete screening of the pelvis is recommended by using ultrasonography, computed tomography (CT) scan, and radiography in patients with a history of chronic constipation from early childhood.

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Year:  2003        PMID: 12861546     DOI: 10.1016/s0022-3468(03)00199-4

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  14 in total

1.  Leiomyomatosis peritonealis disseminata in association with Currarino syndrome?

Authors:  Carmine Nappi; Attilio Di Spiezio Sardo; Vincenzo Dario Mandato; Giuseppe Bifulco; Elisa Merello; Antonio Savanelli; Chiara Mignogna; Valeria Capra; Maurizio Guida
Journal:  BMC Cancer       Date:  2006-05-10       Impact factor: 4.430

2.  Neonatal Currarino's syndrome presenting as intestinal obstruction.

Authors:  Ramnik V Patel; Gregory Shepherd; Hemant Kumar; Nitin Patwardhan
Journal:  BMJ Case Rep       Date:  2013-10-15

Review 3.  Long-term functional outcomes in children with Currarino syndrome.

Authors:  Atsushi Yoshida; Kiki Maoate; Russell Blakelock; Stephen Robertson; Spencer Beasley
Journal:  Pediatr Surg Int       Date:  2010-05-15       Impact factor: 1.827

Review 4.  Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature.

Authors:  Charlotte Schramm; Markus Draaken; Gabriel Tewes; Enrika Bartels; Eberhard Schmiedeke; Stefanie Märzheuser; Sabine Grasshoff-Derr; Stuart Hosie; Stefan Holland-Cunz; Lutz Priebe; Martina Kreiss-Nachtsheim; Per Hoffmann; Stefan Aretz; Markus M Nöthen; Heiko Reutter; Michael Ludwig
Journal:  Eur J Pediatr       Date:  2010-11-02       Impact factor: 3.183

5.  Holoprosencephaly: report of four cases and genotype-phenotype correlations.

Authors:  Francesca Lami; Diana Carli; Paola Ferrari; Monica Marini; Viola Alesi; Lorenzo Iughetti; Antonio Percesepe
Journal:  J Genet       Date:  2013-04       Impact factor: 1.166

6.  Concurrent Hirschsprung's disease and anorectal malformation: a systematic review.

Authors:  Hiroki Nakamura; Prem Puri
Journal:  Pediatr Surg Int       Date:  2019-09-24       Impact factor: 1.827

7.  Congenital funnel anus in children: associated anomalies, surgical management and outcome.

Authors:  Anna Suomalainen; Tomas Wester; Antti Koivusalo; Risto J Rintala; Mikko P Pakarinen
Journal:  Pediatr Surg Int       Date:  2007-12       Impact factor: 1.827

Review 8.  Associations of anorectal malformations and related syndromes.

Authors:  Sam W Moore
Journal:  Pediatr Surg Int       Date:  2013-04-09       Impact factor: 1.827

9.  Currarino's syndrome in twins presenting as neonatal intestinal obstruction--identical presentation in non-identical twins.

Authors:  Ramnik V Patel; Paolo De Coppi; Edward Kiely; Agostino Pierro
Journal:  BMJ Case Rep       Date:  2014-09-08

Review 10.  Association of Hirschsprung's disease and anorectal malformation: a systematic review.

Authors:  Alejandro D Hofmann; Prem Puri
Journal:  Pediatr Surg Int       Date:  2013-09       Impact factor: 1.827

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