Linking animal models to human congenital diaphragmatic hernia

Birth Defects Res A Clin Mol Teratol. 2007 Aug;79(8):565-72. doi: 10.1002/bdra.20370.

Abstract

Background: Congenital diaphragmatic hernia (CDH) is a major life-threatening malformation, occurring in approximately 1 in 3,000 live births. Over the years, different animal models have been used to gain insight into the etiology of this complex congenital anomaly and to develop treatment strategies. However, to date the pathogenic mechanism is still not understood, and treatment remains difficult because of the associated pulmonary hypoplasia and pulmonary hypertension.

Methods: In this review, data available from several animal models will be discussed. The retinoic acid signaling pathway (RA pathway, retinoid pathway) will be addressed as a developmental pathway that is potentially disrupted in the pathogenesis of CDH. Furthermore, genetic factors involved in diaphragm and lung development will be discussed.

Conclusions: With this review article, we aim to provide a concise overview of the current most important experimental genetic data available in the field of CDH.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Diaphragm / abnormalities*
  • Disease Models, Animal*
  • Gene Expression Regulation, Developmental
  • Hernia, Diaphragmatic / etiology*
  • Hernia, Diaphragmatic / metabolism
  • Hernias, Diaphragmatic, Congenital*
  • Humans
  • Mice
  • Mice, Knockout
  • Retinoids / metabolism
  • Signal Transduction

Substances

  • Retinoids