Recurrence of diaphragmatic agenesis associated with multiple midline defects: evidence for an autosomal gene regulating the midline

Am J Med Genet. 1994 Oct 15;53(1):33-8. doi: 10.1002/ajmg.1320530108.

Abstract

We report the familial occurrence of diaphragmatic agenesis in association with other midline anomalies in a brother and sister. Opitz and Gilbert [Am J Med Genet 1982, 12:443-455] introduced the concept of the midline as a developmental field, and there have been reports of pedigrees compatible with the hypothesis of an X-linked gene regulating the development of the midline. This family suggests that an autosomal gene also contributes to the morphogenesis of midline structures.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Anus, Imperforate / genetics
  • Cleft Palate / genetics
  • Diaphragm / abnormalities*
  • Encephalocele / genetics
  • Female
  • Hernia, Umbilical / genetics
  • Humans
  • Male
  • Morphogenesis / genetics*
  • Neural Tube Defects / genetics
  • Pedigree