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Sickle Cell Anemia Testing is a diagnostic test that detects the presence of abnormal hemoglobin responsible for sickle cell anemia. Sickle cell anemia is an inherited blood disorder in which red blood cells become misshapen and break down more easily, leading to various complications. This test helps identify individuals with sickle cell trait or sickle cell disease, enabling appropriate medical management and counseling.
If you reside in Collingdale, Pennsylvania, and have a family history of sickle cell disease or belong to populations with a higher risk of carrying the sickle cell trait, Sickle Cell Anemia Testing is recommended. This includes individuals of African, Mediterranean, Middle Eastern, Indian, and Southeast Asian descent.
Sickle Cell Anemia Testing typically includes the following test:
The interpretation of Sickle Cell Anemia Testing results is based on the presence of abnormal hemoglobin in the blood. A positive result indicates the presence of the sickle cell trait, while a negative result indicates the absence of the trait or disease.
Sickle Cell Anemia Testing is important for:
After Sickle Cell Anemia Testing, healthcare providers review the results with individuals and offer counseling and recommendations based on the findings. Individuals with sickle cell trait or sickle cell disease may receive guidance on managing the condition and minimizing complications.
Sickle Cell Anemia Testing is a crucial tool for detecting sickle cell-related conditions, allowing individuals in Collingdale, Pennsylvania to receive appropriate care and make informed decisions about their health and future.
Updated on Oct 25, 2024
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