Compound heterozygosity for hemoglobin S and hemoglobin E in a family of Proto-Australoid origin: a case report [PDF]
Journal of Medical Case Reports, 2021 Background Hemoglobin S and E are commonly occurring hemoglobin variants among distinctly separate tribal populations of Central and Northeast India, respectively.
Noymi Basumatary +3 more
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Hemoglobin S identification in blood donors: A cross section of prevalence [PDF]
Hematology, Transfusion and Cell Therapy, 2022 Introduction: In Brazil, the sickle cell trait (SCT) has an average prevalence of 4% in the general population and 6–10% among Afro-descendants. Although SCT is highly prevalent, a large segment of the population ignores their status.
Fernanda Lima Kroger +5 more
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Hemoglobin S/OArab: Retinal Manifestations of a Rare Hemoglobinopathy [PDF]
Case Reports in Ophthalmology, 2020 Hemoglobin S/OArab (Hgb S/OArab) disease is a rare hemoglobinopathy which presents similarly to sickle cell retinopathy, with only three prior reports that describe associated retinal findings.
Riley Sanders +5 more
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Scope and efficiency of the newborn screening program in identifying hemoglobin S [PDF]
Revista Brasileira de Hematologia e Hemoterapia, 2014 Background: In 2001, the Brazilian Ministry of Health added hemoglobinopathies to the National Neonatal Screening Program to be implemented in three steps.
Maria Lucia Ivo +5 more
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PB2523: DI-2-ETHYLHEXYL PHTHALATE (DEHP) INHIBITS HEMOGLOBIN S POLYMERIZATION [PDF]
HemaSphere, 2023 Rodrigo Abreu Camacho +9 more
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Stroke From Paradoxical Embolism in a Young Patient With Sickle‐Cell Disease and High Fetal Hemoglobin: A Diagnostic Challenge [PDF]
Clinical Case ReportsSickle‐cell disease (SCD) is characterized by abnormal hemoglobin (Hb) polymerization, leading to erythrocyte sickling and microvascular obstruction.
Yi Hui Luo +5 more
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Hemoglobin S and C affect protein export in Plasmodium falciparum-infected erythrocytes [PDF]
Biology Open, 2015 Malaria is a potentially deadly disease. However, not every infected person develops severe symptoms. Some people are protected by naturally occurring mechanisms that frequently involve inheritable modifications in their hemoglobin.
Nicole Kilian +8 more
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PB2521: STUDY OF HEMOGLOBIN S-OMAN TRAIT: NEW INSIGHTS [PDF]
HemaSphere, 2023 Nouh Al-Mahrouqi +8 more
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Concerted Formation of the Gel of Hemoglobin S [PDF]
Proceedings of the National Academy of Sciences of the United States of America, 1973 Apparent weight-average molecular weights of hemoglobin A and hemoglobin S were measured at high concentrations by equilibrium ultracentrifugation. Carbonmonoxy-hemoglobin S appears to exist as a solution of unassociated molecules, as do carbonmonoxy-and deoxy-hemoglobin A. Deoxy-hemoglobin S, however, exists in a gel-like state at concentrations above
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International Journal of Endorsing Health Science Research, 2021 Background: It has been estimated that 5% of the global population are carriers of Hemoglobin (Hb) disorders. These disorders may cause hemolytic anemia leading to the critical condition of the patients.
Saba Kamil +7 more
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