Clinical and Laboratory Predictors of Elevated TRV In Sickle Cell Anaemia
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چکیده
منابع مشابه
Assessing clinical laboratory funding of Sickle Cell Disease and others associated Disorders in Khuzestan Province
Objective: The aim of this study was to assess clinical laboratory funding for differential diagnosis of sickle cell disease (SCD) and other associated disorders for better understanding of clinical types and prevention of sickling events. Material and Methods: This is a descriptive crossed-sectional study that analyzed the peripheral blood film, sickle cell preparation, hemoglobin electroph...
متن کاملPredicting clinical severity in sickle cell anaemia.
The ability to predict the phenotype of an individual with sickle cell anaemia would allow a reliable prognosis and could guide therapeutic decision making. Some risk factors for individual disease complications are known but are insufficiently precise to use for prognostic purposes; predicting the global disease severity is not yet possible. Genetic association studies, which attempt to link g...
متن کاملSickle Cell Disease and Sickle Cell Anaemia
Sickle cell haemoglobin (HbS) results from an autosomal recessively inherited mutation in which the 17th nucleotide of the beta globin gene is changed from thymine to adenine and the amino acid glutamic acid is replaced by valine at position 6 in the beta globin chain. [1, 2]Sickle cells have a reduced deformability and are easily destroyed, causing occlusion of the microcirculation and a chron...
متن کاملClinical features of pulmonary lesions in sickle-cell anaemia.
Acute pulmonary diseases in patients with sickle-cell anaemia are usually diagnosed as pneumonia, but in our experience their rate of resolution and clinical course is different from pneumonia occurring in patients with normal haemoglobins. To confirm this we analysed the clinical course of these pulmonary episodes in a group of patients with sickle-cell anaemia and compared them with a control...
متن کاملClinical features of sickle cell anaemia in northern nigerian children.
BACKGROUND Sickle cell disease (SCD) is a more common and severe disease in Africa. Nigeria the most populous black nation in Africa has the largest number of sickle cell anaemia (SCA) patients in the world. Borno and Yobe State has the largest number of sickle cell trait in Nigeria with prevalence of 27.9% and 32.6% respectively. Sickle cell anaemia survival to adulthood in Africa was reporte...
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ژورنال
عنوان ژورنال: Journal of Hematology and Oncology Research
سال: 2018
ISSN: 2372-6601
DOI: 10.14302/issn.2372-6601.jhor-18-2139