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Sickle Cell Anemia

Year: 2025

Type: article

Abstract: Sickle-cell anemia (SCA), the most severe form of sickle-cell disease (SCD), is a major hereditary blood disorder characterized by abnormal haemoglobin polymerization, chronic haemolytic anemia, and vaso-occlusive complications. Children with SCA are particularly vulnerable to neurological and cognitive impairments, often resulting from silent cerebral infarctions and cerebrovascular abnormalities.

Source: International Journal of Engineering Development and Research

DOI: 10.56975/ijedr.v13i4.302388

Authors: Raksha.N Raksha.N, Varnikha sri.S, Sarmitha.S Sarmitha.S

Language: English

Topic: Hemoglobinopathies and Related Disorders

Subfield: Genetics

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: hybrid

OpenAlex ID: W4416357716

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