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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
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.
Area of Science:
- Biochemistry
- Genetics
- Pediatrics
Background:
- Hereditary tyrosinemia type 1 (HT-1) results from a deficiency of fumarylacetoacetate hydrolase (FAH), crucial for tyrosine metabolism.
- It follows an autosomal recessive inheritance pattern, making it a rare genetic condition.
- FAH deficiency leads to the accumulation of toxic metabolites, causing severe liver and kidney damage.
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