Severe microcytosis in a hemoglobin E/Β-thalassemia patient with signs of iron deficiency: A case report

BACKGROUND: β-thalassemia is a hereditary disorder characterized by a decrease in the synthesis of β-globin chains that decreases hemoglobin in erythrocytes, low erythrocyte production, and anemia. CASE PRESENTATION: A 6-year-old girl came with complaints of paleness for one week. Physical examinati...

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Detalles Bibliográficos
Autores principales: Goretti, Laurensia, Adiatmaja, Christophorus Oetama, Kahar, Hartono
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207008/
https://www.ncbi.nlm.nih.gov/pubmed/35734663
http://dx.doi.org/10.1016/j.amsu.2022.103826

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207008/
https://www.ncbi.nlm.nih.gov/pubmed/35734663
http://dx.doi.org/10.1016/j.amsu.2022.103826

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