Pediatrics
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18 february 2019 21:01:57 |
| Hb Knossos (HBB: c.82G > T), ?-globin CD 5 (-CT) (HBB: c.17_18delCT) and ?-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with ?-thalassemia intermedia (BMC Pediatrics) |
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Tweet Beta thalassemia (?-thal) is an inherited hemoglobin disorder characterized by reduced synthesis of the hemoglobin that results in microcytic hypochromic anemia. ?-Thalassemia intermedia (TI) is a clinical ter... |
| 61 viewsCategory: Pediatrics |
 A de novo ANK1 mutation associated to hereditary spherocytosis: a case report (BMC Pediatrics)Gastric MALT lymphoma presented with primary perforation in an adolescent: a case report (BMC Pediatrics) 
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