FEATURES OF THE COURSE AND LABORATORY DIAGNOSIS OF SICKLE CELL ANEMIA

Ibragimova Nadiya Sabirovna; Aliyeva Nilufar

Authors

Ibragimova Nadiya Sabirovna Assistant of the Department of Clinical and Laboratory Diagnostics with a Course of Clinical and Laboratory Diagnostics at the Faculty of Postgraduate Education
Aliyeva Nilufar Cadet of the Department of Clinical and Laboratory Diagnostics with a Course of Clinical and Laboratory Diagnostics of FOPE, Samarkand State Medical University, Uzbekistan, Samarkand

Keywords:

Sickle cell anemia, clinical symptoms, laboratory diagnostics, treatment

Abstract

Sickle cell anemia is one of the most pressing diseases in the field of hemato-oncology, affecting millions of people worldwide. This hereditary disease, caused by a mutation in the gene responsible for the synthesis of beta-globin, leads to a change in the shape of red blood cells, which in turn causes their abnormal aggregation, impeding blood circulation and reducing the level of oxygen in the tissues. The relevance of the problem lies not only in the high prevalence of the disease, but also in the complexity of its diagnosis and treatment. This hereditary disease, caused by a mutation in the gene responsible for the synthesis of beta-globin, leads to a change in the shape of red blood cells, which in turn causes their abnormal aggregation, impeding blood circulation and reducing the level of oxygen in the tissues. The relevance of the problem lies not only in the high prevalence of the disease, but also in the complexity of its diagnosis and treatment.