Hereditary Tyrosinemia Type-1 With Late Presentation: A Case Report

Md Ilyaz1, Renuka S Jadhav1, Vineeta Pande1

  • 1Pediatrics, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.

Cureus
|July 25, 2024
PubMed
Summary

Hereditary tyrosinemia type 1 (HT-1) is a rare genetic disorder caused by a deficiency in the fumarylacetoacetate hydrolase (FAH) enzyme. This case highlights a child with HT-1 managed with nitisinone and dietary restrictions pending liver transplant.

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