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Hb E disease / trait is a qualitative hemoglobinopathy, due to substitution of lysine for glutamic acid in 26th position og beta globin chain. These diseases are caused by mutations affecting the genes encoding the globin chains of the hemoglobin molecules. | Kids Talk Hour - Dr Asma Akhter
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Hb E disease / trait is a qualitative hemoglobinopathy, due to substitution of lysine for glutamic acid in 26th position og beta globin chain. These diseases are caused by mutations affecting the genes encoding the globin chains of the hemoglobin molecules. | Kids Talk Hour - Dr Asma Akhter
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🏵️ Homozygous Hemoglobin E 🏵️ 🔹 Genotype: Abnormality in the structure of the beta-globin chain (β-globin). Two Hemoglobin E genes (βE/βE) 🔹Individuals can inherit the βE gene from both parents. 🔹Hb Type: EE (Hb E ≥ 80% and Hb F ≤ 5%) 🔹RBC 🔸Distinctive Features : Target cell 🔸Other : Microcyte , Poikilocytosis Share Knowledge and Answer questions for Hematology and all Medical Technology https://www.facebook.com/rose.apple.127/subscribe/ #Thalassemia #HomoE #Hematology #reels | RoseApple
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🏵️ Homozygous Hemoglobin E 🏵️ 🔹 Genotype: Abnormality in the structure of the beta-globin chain (β-globin). Two Hemoglobin E genes (βE/βE) 🔹Individuals can inherit the βE gene from both parents. 🔹Hb Type: EE (Hb E ≥ 80% and Hb F ≤ 5%) 🔹RBC 🔸Distinctive Features : Target cell 🔸Other : Microcyte , Poikilocytosis Share Knowledge and Answer questions for Hematology and all Medical Technology https://www.facebook.com/rose.apple.127/subscribe/ #Thalassemia #HomoE #Hematology #reels | RoseApple
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