[Recommendations and management of type I hereditary or hepatorenal tyrosinemia]

An Pediatr (Barc). 2010 Nov;73(5):279.e1-4. doi: 10.1016/j.anpedi.2010.03.005. Epub 2010 Sep 1.
[Article in Spanish]

Abstract

Tyrosinemia type I is a potentially lethal disease if not diagnosed and treated properly. Diagnostic and therapeutic advances in recent years have significantly improved the prognosis for these patients. It is therefore important that the pediatrician has a clinical practice guideline with recommendations for diagnosis and treatment of this disease that leads to the appropriate intervention.

Publication types

  • English Abstract

MeSH terms

  • Child
  • Humans
  • Practice Guidelines as Topic
  • Tyrosinemias / diagnosis
  • Tyrosinemias / therapy