Results 31 to 40 of about 1,304,324 (179)
Revista Brasileira de Hematologia e Hemoterapia, 2014 Objectives: To analyze the frequency of βS-globin haplotypes and alpha-thalassemia, and their influence on clinical manifestations and the hematological profile of children with sickle cell anemia. Method: The frequency of βS-globin haplotypes and alpha-
Roberta Faria Camilo-Araújo +4 more
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Prolonged Pyrexia: Kikuchi-Fujimoto Disease in a Patient With Hb H-Constant Spring Thalassemia
Clinical Medicine Insights: Case Reports, 2020 Introduction: Haemoglobin H (Hb H) disease is an alpha thalassemia characterised by either 3 alpha-globin gene deletions (deletional type) or 2 alpha-globin gene deletions with 1-point mutation (nondeletional type).
Ganesh Kasinathan
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Journal of clinical laboratory analysis (Print), 2021 Thalassemia is a group of inherited autosomal recessive hemolytic anemia disease caused by reduced or absent synthesis of globin chain/chains of hemoglobin. Only few studies showed the molecular characterization of α‐ and β‐thalassemia in Meizhou city of
Heming Wu +3 more
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Anemia, 2015 Background. Nontransfusion dependent thalassemia (NTDT) is a milder form of thalassemia that does not require regular transfusion. It is associated with many complications, which differ from that found in transfusion-dependent thalassemia (TDT ...
Poramed Winichakoon +7 more
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Thalassemia, a human blood disorder
Brazilian Journal of Biology, 2021 A group of inherited blood defects is known as Thalassemia is among the world’s most prevalent hemoglobinopathies. Thalassemias are of two types such as Alpha and Beta Thalassemia. The cause of these defects is gene mutations leading to low levels and/or
F. Shafique +8 more
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Awareness of the Thalassemic Patients’ Parents toward Thalassemia in Kirkuk City [PDF]
مجلة الموصل للتمريض, 2014 Background and objectives:- Thalassemia is a blood disorder passed down through families (inherited) in which the body makes an abnormal form of hemoglobin, the protein in red blood cells that carries oxygen.
Yousif Abdulmuhsin Salih
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Mediterranean Journal of Hematology and Infectious Diseases, 2023 Background and objectives. Investigating the prevalence of thalassemia in the Vietnamese population, building a clinical decision support system for prenatal screening for thalassemia. Methods.
Danh Cuong Tran +7 more
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Update in Laboratory Diagnosis of Thalassemia
Frontiers in Molecular Biosciences, 2020 Alpha- and β-thalassemias and abnormal hemoglobin (Hb) are common in tropical countries. These abnormal globin genes in different combinations lead to many thalassemic diseases including three severe thalassemia diseases, i.e., homozygous β-thalassemia ...
Thongperm Munkongdee +4 more
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Thalassemia intermedia as a result of heterozygosis for ß0-thalassemia and aaaanti-3.7/aa genotype in a Brazilian patient [PDF]
Brazilian Journal of Medical and Biological Research, 2003 We report a case in which the interaction of heterozygosis for both the ß0-IVS-II-1 (G->A) mutation and the aaaanti-3.7 allele was the probable cause for the clinical occurrence of thalassemia intermedia.
E.M. Kimura +4 more
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Alpha Thalassemia in Istanbul: Distribution of Deletions in Alpha-globin Gene Cluster
Genel Tıp DergisiBackground/Aims: Alpha thalassemia is an autosomal recessive congenital disease resulting from a globin protein disorder encoded by genes in the alpha thalassemia gene cluster.
Fatma Nihal Öztürk
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