Literature DB >> 2061816

Familial Hirschsprung's disease: report of autosomal dominant and probable recessive X-linked kindreds.

V A Stannard1, C Fowler, L Robinson, G Besner, P L Glick, J E Allen, T C Jewett, D R Cooney.   

Abstract

Multifactorial sex-modified inheritance has been proposed as the model of transmission in familial Hirschsprung's disease (HD). A review of two separate kindreds suggests that aganglionosis may be inherited as an X-linked recessive or an autosomal dominant trait. Chromosomal anomalies and other syndromes, including G6PD deficiency, may occur with familial HD. Recurrence risk counseling for family members depends on accurate pedigree analysis and a comprehensive understanding of the genetic factors involved.

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Year:  1991        PMID: 2061816     DOI: 10.1016/0022-3468(91)90714-5

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


  5 in total

Review 1.  The RET proto-oncogene: a challenge to our understanding of disease pathogenesis.

Authors:  T Kusafuka; P Puri
Journal:  Pediatr Surg Int       Date:  1997       Impact factor: 1.827

Review 2.  Hirschprung's disease.

Authors:  P B Sullivan
Journal:  Arch Dis Child       Date:  1996-01       Impact factor: 3.791

Review 3.  Hirschsprung's disease: clinical and experimental observations.

Authors:  P Puri
Journal:  World J Surg       Date:  1993 May-Jun       Impact factor: 3.352

Review 4.  Hirschsprung's disease in twins: a systematic review and meta-analysis.

Authors:  D Henderson; J Zimmer; H Nakamura; Prem Puri
Journal:  Pediatr Surg Int       Date:  2017-06-10       Impact factor: 1.827

5.  Familial Near-Total Intestinal Aganglionosis.

Authors:  Hidouri Saida; Zitouni Hayet; Chahed Jamila; Mosbahi Sana; Belhassen Samia; Ksiaa Amine; Hmida Badii; Krichene Imed; Sahnoun Lassad; Mekki Mongi; Belguith Mohsen; Nouri Abdellatif
Journal:  J Neonatal Surg       Date:  2017-08-10
  5 in total

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