Literature DB >> 1552451

Hirschsprung's disease: associated abnormalities and demography.

E T Ryan1, J L Ecker, N A Christakis, J Folkman.   

Abstract

We here examine the demographic parameters of patients with Hirschsprung's disease. The study population includes all patients with histologically confirmed disease treated at the Children's Hospital Medical Center of Boston over the 25-year period extending from 1961 through the first quarter of 1986. There were 179 cases. Overall, children with Hirschsprung's disease were found less likely to be first born (P less than .01). This relationship was seen to persist irrespective of maternal age, maternal race, or type of disease. The implications of this finding are discussed. Overall, 22% of these children had one or more associated abnormalities involving the neurological, cardiovascular, urological, and gastrointestinal systems. Many of the disorders appeared to be related to neurocrestopathies. Frequent associations included Down's syndrome, defects in cardiac septation, tetralogy of Fallot, and Dandy-Walker syndrome. These conditions occurred more frequently than would have been predicted through chance alone. This study found no association between an increased maternal age and the occurrence of Hirschsprung's disease. This study also found that approximately 7% of the affected children had been born prematurely.

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Year:  1992        PMID: 1552451     DOI: 10.1016/0022-3468(92)90111-j

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


  19 in total

Review 1.  Hirschsprung disease, associated syndromes, and genetics: a review.

Authors:  J Amiel; S Lyonnet
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

2.  [Twenty years diagnostic competence center for Hirschsprung's disease in Basel].

Authors:  E Bruder; W A Meier-Ruge
Journal:  Chirurg       Date:  2010-06       Impact factor: 0.955

Review 3.  Syndromic Hirschsprung's disease and associated congenital heart disease: a systematic review.

Authors:  Johannes W Duess; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-07-09       Impact factor: 1.827

Review 4.  Familial Hirschsprung's disease: a systematic review.

Authors:  Danielle Mc Laughlin; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-07-16       Impact factor: 1.827

5.  Hirschsprung's disease: the Australian Paediatric Surveillance Unit's experience.

Authors:  S J Singh; G D H Croaker; P Manglick; C L Wong; H Athanasakos; E Elliott; D Cass
Journal:  Pediatr Surg Int       Date:  2003-04-03       Impact factor: 1.827

Review 6.  Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung's disease: a systematic review.

Authors:  Alejandro D Hofmann; Johannes W Duess; Prem Puri
Journal:  Pediatr Surg Int       Date:  2014-06-29       Impact factor: 1.827

Review 7.  Prevalence of Hirschsprung's disease in premature infants: a systematic review.

Authors:  Johannes W Duess; Alejandro D Hofmann; Prem Puri
Journal:  Pediatr Surg Int       Date:  2014-07-02       Impact factor: 1.827

8.  A meta-analysis of clinical outcome in patients with total intestinal aganglionosis.

Authors:  Elke Ruttenstock; Prem Puri
Journal:  Pediatr Surg Int       Date:  2009-10       Impact factor: 1.827

Review 9.  Total colonic aganglionosis: a systematic review and meta-analysis of long-term clinical outcome.

Authors:  Danielle Mc Laughlin; Florian Friedmacher; Prem Puri
Journal:  Pediatr Surg Int       Date:  2012-08       Impact factor: 1.827

Review 10.  The developmental etiology and pathogenesis of Hirschsprung disease.

Authors:  Naomi E Butler Tjaden; Paul A Trainor
Journal:  Transl Res       Date:  2013-03-22       Impact factor: 7.012

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