Literature DB >> 124513

[Incidence and etiology of omphaloceles (author's transl)].

H D Rott.   

Abstract

Omphaloceles are congenital malformations with herniation of the abdominal viscera into the umbilical cord. The incidence in newborns is 1:4300, the sex ratio 1.24:1 in favour to boys. Children with this malformation are neither more frequent at the beginning nor at the end of the sibship; the average maternal age is not increased. In about 50% other different malformations are found. All those omphaloceles, which are found as an obligatory symptom in the EMG syndrome (Wiedemann-Beckwith syndrome) to be probably in most cases autosomal recessively inherited or which are seen within a chromosomal malformation syndrome are of etiologically known origin. Omphaloceles without other malformations are mainly sporadic, less frequent in sibs, possibly due to a polygenic or multifactorial mode of inheritance. Findings in population genetics and animal experiments suggest that exogenous factors, too, can be the cause of malformation syndromes with omphaloceles.

Entities:  

Mesh:

Year:  1975        PMID: 124513

Source DB:  PubMed          Journal:  Z Kinderheilkd        ISSN: 0044-2917


  3 in total

1.  Interrelationship of different dysraphic malformations and consequences for genetic counselling.

Authors:  J U Walther
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

2.  Tuberous sclerosis and dysplasia of the corpus callosum. Case report of their combined occurrence in a newborn.

Authors:  P G Barth; F C Stam; J J von der Harten
Journal:  Acta Neuropathol       Date:  1978-04-26       Impact factor: 17.088

3.  Etiological study of omphalocele.

Authors:  A Czeizel; M Vitéz
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

  3 in total

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