p.Gly693Arg Homozygote Mutation in Dubin-Johnson Syndrome with Atypical Liver Biopsy due to Reactivation of Hepatitis B Concomitant with Persistent Loss of Kidney Function
Dubin-Johnson syndrome is a rare genetic disease that causes impaired transport of bilirubin. In most cases, there will be no symptoms. However, some people might develop jaundice due to certain conditions. In this case, we would like to present a 54-year-old male patient with Dubin-Johnson syndrom...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Interna Publishing
2025-10-01
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| coleção: | Acta Medica Indonesiana |
| Assuntos: | |
| Acesso em linha: | https://actamedindones.org/index.php/ijim/article/view/2938 |
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