Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report

INTRODUCTION: Hereditary hemochromatosis is an inherited disorder of iron metabolism, characterized by excessive iron deposition in major organs of the body, leading to multi-organ dysfunction. It is a genetically heterogeneous disease caused by mutations in one or more different genes, the most com...

Descripción completa

Detalles Bibliográficos
Autores principales: Wickramasinghe, Wasanthi, Karunathilaka, Chathurika, Jayasinghe, Saroj, Gooneratne, Lallindra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346448/
https://www.ncbi.nlm.nih.gov/pubmed/32641120
http://dx.doi.org/10.1186/s13256-020-02428-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346448/
https://www.ncbi.nlm.nih.gov/pubmed/32641120
http://dx.doi.org/10.1186/s13256-020-02428-3

Ejemplares similares