Diagnostic and Therapeutic Challenges of Hereditary Tyrosinemia Type 1 in Lebanon: A 12-Year Retrospective Review

Background: Hereditary tyrosinemia type 1 is a rare genetic disorder leading to liver cirrhosis and hepatocellular carcinoma. Few decades ago, dietary measures and ultimately liver transplant constituted the only treatment modalities. Nowadays, early diagnosis and therapy with nitisinone can reverse...

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Detalles Bibliográficos
Autores principales: Daou, Karim N., Barhoumi, Abir, Bassyouni, Amina, Karam, Pascale E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377248/
https://www.ncbi.nlm.nih.gov/pubmed/34422723
http://dx.doi.org/10.3389/fped.2021.698577

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8377248/
https://www.ncbi.nlm.nih.gov/pubmed/34422723
http://dx.doi.org/10.3389/fped.2021.698577

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