HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Neonatal liver failure: a genetic and metabolic perspective.

Abstract
Liver failure in newborns can present formidable diagnostic challenges. The presentation of neonatal liver failure is variable and the initial assessment is crucial in the determination of potentially treatable causes. We present a case of neonatal hemochromatosis, review genetic and metabolic causes of neonatal liver failure, and outline an updated differential diagnosis of neonatal liver failure. In addition, we propose a comprehensive initial work-up of neonatal liver failure, and review current treatments for neonatal hemochromatosis.
AuthorsMargarita Sifuentes Saenz, Johan Van Hove, Gunter Scharer
JournalCurrent opinion in pediatrics (Curr Opin Pediatr) Vol. 22 Issue 2 Pg. 241-5 (Apr 2010) ISSN: 1531-698X [Electronic] United States
PMID20090522 (Publication Type: Case Reports, Journal Article, Review)
Topics
  • Hemochromatosis (diagnosis)
  • Humans
  • Infant, Newborn
  • Liver Failure (diagnosis, genetics, metabolism)
  • Male

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: