Familial occurrence of omphalocele suggesting sex-linked inheritance

Arch Dis Child. 1979 Feb;54(2):142-3. doi: 10.1136/adc.54.2.142.

Abstract

A family is described in which 4 males in two generations had omphalocele. There was no case of omphalocele in any of the women. It is suggested that the mode of inheritance could be a sex-linked recessive trait.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Female
  • Hernia, Umbilical / genetics*
  • Humans
  • Infant, Newborn
  • Male
  • Pedigree
  • Sex Chromosome Aberrations