Cargando…

A rare case of coinheritance of Hemoglobin H disease and sickle cell trait combined with severe iron deficiency

We present a case of a 40-year-old female from Turkey, who was referred to our outpatient clinic for an undetermined thalassemia and sickle cell trait. At first consultation hemoglobin was decreased (71 g/L) with microcytosis (MCV 55.1 fL), and hypochromia (MCHC 239 g/L). The patient had severe iron...

Descripción completa

Detalles Bibliográficos
Autores principales:	Medinger, Michael, Saller, Elisabeth, Harteveld, Cornelis L, Lehmann, Thomas, Graf, Lukas, Rovo, Alicia, Buser, Andreas, Passweg, Jakob, Tichelli, André
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	PAGEPress Publications 2011
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269802/ https://www.ncbi.nlm.nih.gov/pubmed/22593821 http://dx.doi.org/10.4081/hr.2011.e30

Ejemplares similares

Comparison of a powered bone marrow biopsy device with a manual system: results of a prospective randomised controlled trial
por: Bucher, Christoph Marcus, et al.
Publicado: (2013)

Coinheritance of B-Thalassemia and Sickle Cell Anaemia in Southwestern Nigeria
por: Vincent, Osunkalu, et al.
Publicado: (2016)

Hemoglobin S and Glucose-6-Phosphate Dehydrogenase Deficiency Coinheritance in AS and SS Individuals in Malaria-Endemic Region: A Study in Calabar, Nigeria
por: Okafor, Ifeyinwa M., et al.
Publicado: (2019)

Coinheritance of hemoglobin D-Punjab and β(0)-thalassemia 3.4 kb deletion in a Thai girl
por: Panyasai, Sitthichai, et al.
Publicado: (2017)

The odds and implications of coinheritance of hemophilia A and B
por: Karch, Corinne, et al.
Publicado: (2020)

Very long-term follow-up of aplastic anemia treated with immunosuppressive therapy or allogeneic hematopoietic cell transplantation
por: Drexler, Beatrice, et al.
Publicado: (2020)

Angiogenesis in myeloproliferative neoplasms, new markers and future directions
por: Medinger, Michael, et al.
Publicado: (2014)

Iron Depletion: An Ameliorating Factor for Sickle Cell Disease?
por: Giordano, P. C., et al.
Publicado: (2011)

Increase of Suicide and Accidental Death After Hematopoietic Stem Cell Transplantation: A Cohort Study on Behalf of the Late Effects Working Party of the European Group for Blood and Marrow Transplantation (EBMT)
por: Tichelli, André, et al.
Publicado: (2013)

Novel therapeutic options in Acute Myeloid Leukemia
por: Medinger, Michael, et al.
Publicado: (2016)

Influence of HLA-DPB1 mismatches on outcome after allogeneic hematopoietic stem cell transplantation
por: Hunziker, Mireille, et al.
Publicado: (2021)

Coinheritance of beta-thalassemia minor and hereditary pyropoikilocytosis: case report
por: Naoum, Flávio Augusto, et al.
Publicado: (2020)

Sickle Cell Disease and Fetal Hemoglobin
por: Rivera, Alicia
Publicado: (2018)

Adding eltrombopag to immunosuppression: the importance of predicting outcome
por: Tichelli, André, et al.
Publicado: (2022)

Pathogenesis of Acquired Aplastic Anemia and the Role of the Bone Marrow Microenvironment
por: Medinger, Michael, et al.
Publicado: (2018)

Characterization of engraftment dynamics in myelofibrosis after allogeneic hematopoietic cell transplantation including novel conditioning schemes
por: Jungius, Sarah, et al.
Publicado: (2023)

Case Report: Coinheritance of Germline Mutations in APC and BRCA1 in Colorectal Cancer
por: Huang, Wei, et al.
Publicado: (2021)

Allogeneic hematopoietic stem cell transplantation in non‐Hodgkin lymphoma in Switzerland, 30 years of experience: Sooner is better
por: Rebmann, Ekaterina, et al.
Publicado: (2022)

Impact of Sickle Cell Trait Hemoglobin on the Intraerythrocytic Transcriptional Program of Plasmodium falciparum
por: Saelens, Joseph W., et al.
Publicado: (2021)

Coinheritance of hereditary spherocytosis and reversibility of cirrhosis in a young female patient with hereditary hemochromatosis
por: Höblinger, A, et al.
Publicado: (2009)

THE STATE OF HEMOGLOBIN IN SICKLED ERYTHROCYTES
por: Stetson, Chandler A.
Publicado: (1966)

Sideroblastic changes of the bone marrow can be predicted by the erythrogram of peripheral blood
por: ROVÓ, A, et al.
Publicado: (2010)

Prevalence of Sickle Cell Trait and Rare Hemoglobin Variants in the Metropolitan Washington DC Area
por: Niu, Xiaomei, et al.
Publicado: (2020)

Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes
por: Forte, Giovanna, et al.
Publicado: (2022)

Low Incidence of hepatic sinusoidal obstruction syndrome/veno-occlusive disease in adults undergoing allogenic stem cell transplantation with prophylactic ursodiol and low-dose heparin
por: Stutz, Lina, et al.
Publicado: (2022)

Coexisting Iron Deficiency Anemia and Beta Thalassemia Trait: Effect of Iron Therapy on Red Cell Parameters and Hemoglobin Subtypes
por: Verma, Sarika, et al.
Publicado: (2014)

Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease
por: Lennon, Rachel, et al.
Publicado: (2015)

Biomarkers in Tumor Angiogenesis and Anti-Angiogenic Therapy
por: Pircher, Andreas, et al.
Publicado: (2011)

Pitfalls of Measuring Hemoglobin A1c in a Patient with Sickle Cell Trait in South Korea
por: Yang, Ji Hyun, et al.
Publicado: (2019)

Sickle-trait hemoglobin reduces adhesion to both CD36 and EPCR by Plasmodium falciparum-infected erythrocytes
por: Petersen, Jens E. V., et al.
Publicado: (2021)

GELS OF NORMAL AND SICKLED HEMOGLOBIN : COMPARATIVE STUDY
por: White, James G., et al.
Publicado: (1970)

The rare hemoglobin variant Hb Mizuho: report of a Swiss family and literature review
por: Njue, Linet, et al.
Publicado: (2021)

Antisickling Drugs Targeting βCys93 Reduce Iron Oxidation and Oxidative Changes in Sickle Cell Hemoglobin
por: Kassa, Tigist, et al.
Publicado: (2019)

Hematological, Biochemical Properties, and Clinical Correlates of Hemoglobin S Variant Disorder: A New Insight Into Sickle Cell Trait
por: Khaled, Safaa A.A., et al.
Publicado: (2022)

New Role for Cdc14 Phosphatase: Localization to Basal Bodies in the Oomycete Phytophthora and Its Evolutionary Coinheritance with Eukaryotic Flagella
por: Ah-Fong, Audrey M. V., et al.
Publicado: (2011)

PB2317: COINHERITANCE OF COMBINED FACTOR VII AND FACTOR XIII DEFICIENCY IS ASSOCIATED WITH A MILD BLEEDING PHENOTYPE IN PATIENT WITH NON-TRANSFUSION DEPENDENT THALASSEMIA
por: Alshareef, O., et al.
Publicado: (2022)

Long-term outcome of a randomized controlled study in patients with newly diagnosed severe aplastic anemia treated with antithymocyte globulin and cyclosporine, with or without granulocyte colony-stimulating factor: a Severe Aplastic Anemia Working Party Trial from the European Group of Blood and Marrow Transplantation
por: Tichelli, André, et al.
Publicado: (2020)

Glycosylated Hemoglobin in Subjects Affected by Iron-Deficiency Anemia
por: Intra, Jari, et al.
Publicado: (2019)

Fetal hemoglobin and hemolysis markers in sickle cell anemia()
por: Colella, Marina Pereira, et al.
Publicado: (2015)

Rapid and inefficient kinetics of sickle hemoglobin fiber growth
por: Castle, Brian T., et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_i7r4tbftsm4p1thcaqg7q63d09