Hemoglobin Reims—a rare alpha globin chain variant and its interaction with beta thalassemia
Authors (first, second and last of 6)
Collection
Hemoglobinopathies and other benign red blood cell disorders
Hemoglobinopathies and other benign red blood cell disorders are encountered by diagnostic hematopathologists and by hematologists mainly on examination of patient samples from peripheral blood and bone marrow.
This collection will include original articles, case reports, review articles, images, letters to the editor and editorials on various non-neoplastic disorders that cause decreased red blood cell production by ineffective erythropoiesis (e.g., megaloblastic anemia, iron deficiency anemia, etc.), that produce hemolytic anemia by intrinsic red blood cell (RBC) defects (e.g., hemoglobinopathies, membranopathies, enzyme disorders, etc.) or by extrinsic RBC defects (autoimmune hemolytic anemias), or that result in secondary erythrocytoses. Also included are papers on automated analyzers and on ancillary techniques that may aid the process of diagnosing these RBC disorders. Future published submissions on hemoglobinopathies and other benign RBC disorders will be added to this collection. We welcome your contribution.
Articles (15 in this collection)
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Co-inheritance of Hb Ottawa and HbS: a rare interaction leading to an interesting diagnostic challenge
Authors (first, second and last of 7)
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Extramedullary hematopoiesis in β-thalassemia major patient: a case report and review of the literature
Authors (first, second and last of 5)
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A multi-centre case series of alectinib-related erythrocyte membrane changes and associated haemolysis
Authors (first, second and last of 5)
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HBB gene mutation spectrum in an Indian cohort of 1530 cases using an in-house targeted next-generation sequencing assay
Authors (first, second and last of 13)
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Prevalence of β-haemoglobinopathies in Eastern India and development of a novel formula for carrier detection
Authors (first, second and last of 4)
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Reticulocyte count and its parameters: comparison of automated analyzers, flow cytometry, and manual method
Authors (first, second and last of 5)
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When the diagnosis is difficult to digest: severe vitamin B12 deficiency secondary to pernicious anemia mimicking life-threatening thrombotic thrombocytopenic purpura
Authors (first, second and last of 7)
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