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Double trouble: A case of fraternal twins with iron‐refractory iron‐deficiency anemia

Iron‐refractory iron‐deficiency anemia (IRIDA) is a rare autosomal recessive disease that presents in childhood. We report the case of fraternal twins presenting with severe hypochromic microcytic anemia and hypoferritinemia. Two missense mutations affecting the TRMPSS6 gene were identified, consist...

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Detalles Bibliográficos
Autores principales:	Malherbe, Jacques A. J., Cole, Catherine H.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558572/ https://www.ncbi.nlm.nih.gov/pubmed/36254154 http://dx.doi.org/10.1002/ccr3.6401

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