Juvenile Hemochromatosis: Rheumatic Manifestations of 2 Sisters Responding to Deferasirox Treatment. A Case Series and Literature Review

Hereditary hemochromatosis (HH) is an inherited iron overload. The most common form of HH is type 1 hereditary hemochromatosis (HFE-related), which is associated with mutation of the HFE gene located on chromosome 6 and inherited in an autosomal recessive pattern. Type 2 hereditary hemochromatosis o...

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Detalles Bibliográficos
Autores principales: Alqanatish, Jubran, Alsowailmi, Banan, Alfarhan, Haneen, Alhamzah, Albandari, Alharbi, Talal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815067/
https://www.ncbi.nlm.nih.gov/pubmed/33488128
http://dx.doi.org/10.2147/OARRR.S276112

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815067/
https://www.ncbi.nlm.nih.gov/pubmed/33488128
http://dx.doi.org/10.2147/OARRR.S276112

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