Results 11 to 20 of about 2,702 (213)
Orphanet Journal of Rare Diseases, 2010 Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of hemoglobin resulting in variable phenotypes ranging from severe anemia to clinically asymptomatic individuals. The total annual incidence of symptomatic individuals is estimated at 1 in 100,000 throughout the world and 1 in 10 ...
Galanello R, ORIGA, RAFFAELLA
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Thalassemia (Beta-Thalassemia)
International Journal For Multidisciplinary Research, 2023 Thalassemia is an inherited blood disorder characterized by less oxygen carrying protein (Haemoglobin) and fever red blood cells in the body than normal. There are mainly two types of thalassemia i.e. Alpha and Beta thalassemia about 1-5% of the global population 80-90 million people are the carrier of ß thalassemia which is major concern.
Tathe Pratiksha Annasaheb - +2 more
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Unstable Hemoglobin, a Rare but Significant Cause of Hemolytic Anemia: Recognition of Peripheral Smear Findings Is Crucial for Diagnosis. [PDF]
Int J Lab HematolInternational Journal of Laboratory Hematology, Volume 48, Issue 2, Page 237-239, April 2026.
Shean RC, Agarwal A, Rets AV.
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Pediatrics In Review, 2012 Thalassemia is the most common form of inherited anemia worldwide. The World Health Organization reports suggest that about 60,000 infants are born with a major thalassemia every year. Although individuals originating from the tropical belt are most at risk, it is a growing global health problem due to extensive population migrations. Despite important
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Non-transfusion-dependent thalassemias
Haematologica, 2013 Non-transfusion-dependent thalassemias include a variety of phenotypes that, unlike patients with beta (β)-thalassemia major, do not require regular transfusion therapy for survival.
Khaled M. Musallam +3 more
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Revista Brasileira de Hematologia e Hemoterapia, 2007 Há vários tipos de hemoglobinopatias que são caracterizados por variantes das hemoglobinas anormais (ex: Hb S, Hb C, Hb Instáveis,etc) e por talassemias (ex: tal. alfa, tal.
Paulo Cesar Naoum +1 more
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Hemoglobinopathies in Iran: An Updated Review
International Journal of Hematology-Oncology and Stem Cell Research, 2020 Hemoglobinopathies are the most common single gene disorders (monogenic disorders) in the world population. Due to specific position of Iran and the presence of multi-ethnic groups in the country, there are many varieties in the molecular genetics and ...
Abolfazl Nasiri +2 more
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Revista Brasileira de Hematologia e Hemoterapia, 2006 As anemias hereditárias, que englobam as hemoglobinopatias e talassemias são doenças determinadas geneticamente. Na maioria dos casos os heterozigotos são assintomáticos e desconhecem o defeito genético do qual são portadores.
Paulo R. Melo-Reis +5 more
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Thalassemia ENDOCRINOPATHIES IN THALASSEMIA PATIENTS
PAFMJ, 2021 Objective: To determine the common endocrine complications found in children having thalassemia major. Study Design: Cross-sectional study. Place and Duration of Study: Department of Pediatric Medicine, Combined Military Hospital Multan, from May to Nov 2019. Methodology: A total of 160 Children with thalassemia were taken in this ...
Umer Touheed +5 more
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Revista Brasileira de Hematologia e Hemoterapia, 2008 O diagnóstico neonatal de hemoglobinopatias permite a melhoria na qualidade de vida do doente com a implementação de medidas profiláticas, acompanhamento clínico e aconselhamento genético.
Luciane M. S. Melo +3 more
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