FOXF1 Gene Mutation in Alveolar Capillary Dysplasia Associated With Hirschsprung's Disease and Clinical Review

J Paediatr Child Health. 2016 Jul;52(7):787-8. doi: 10.1111/jpc.13191.

Publication types

  • Case Reports

MeSH terms

  • Comorbidity
  • Fatal Outcome
  • Female
  • Forkhead Transcription Factors / genetics*
  • Hirschsprung Disease / genetics*
  • Humans
  • Infant, Newborn
  • Mutation / genetics*
  • Persistent Fetal Circulation Syndrome / genetics*
  • Pulmonary Alveoli / abnormalities*

Substances

  • FOXF1 protein, human
  • Forkhead Transcription Factors

Supplementary concepts

  • Alveolar capillary dysplasia