Dubin-Johnson Syndrome: A Case Report

Dubin-Johnson syndrome (DJS) is a rare autosomal recessive genetic disease caused by mutations in the bilirubin transporter MRP2. It is characterized by recurrent episodes of jaundice and conjugated hyperbilirubinemia. Numerous instances of hyperbilirubinemia disorders resembling Dubin-Johnson syndr...

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Detalles Bibliográficos
Autores principales: Siddiqui, Abdul Hannan, Alsabe, Muhammad R, Tehseen, Zuha, Hatamleh, Modather I, Taslim, Sanzida, Abdelrahman, Ameer, Saleem, Faraz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099096/
https://www.ncbi.nlm.nih.gov/pubmed/37065356
http://dx.doi.org/10.7759/cureus.36115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099096/
https://www.ncbi.nlm.nih.gov/pubmed/37065356
http://dx.doi.org/10.7759/cureus.36115

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