A new genetic mutation in a patient with syndromic diarrhea and hepatoblastoma

J Pediatr Gastroenterol Nutr. 2013 Sep;57(3):e15. doi: 10.1097/MPG.0b013e31825600c4.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Diarrhea / genetics*
  • Diarrhea, Infantile / genetics*
  • Facies
  • Fatal Outcome
  • Female
  • Fetal Growth Retardation / genetics*
  • Genetic Loci*
  • Hair Diseases / genetics*
  • Hepatoblastoma / genetics*
  • Humans
  • Infant
  • Liver Neoplasms / genetics*
  • Mutation*

Supplementary concepts

  • Trichohepatoenteric Syndrome