Written by: Dr Subita Alagh
19 June 2025
Sickle cell disease is a genetic blood disorder where red blood cells become C-shaped instead of round. These sickle-shaped cells can block blood flow and break down faster, leading to pain and anemia.
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It starts with a gene. You inherit the disease when both parents pass down the sickle cell gene. These genes make the body produce abnormal hemoglobin, which causes red cells to change shape and get stuck in blood vessels.
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The most common signs are pain (called a pain crisis) and anemia. Crises can be triggered by cold, dehydration, or stress, or appear without a cause. Anemia leads to fatigue, breathlessness, and paleness.
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– Tiredness – Pale skin or lips – Dizziness or irritability – Trouble focusing – Yellowing eyes (jaundice)
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Most are diagnosed at birth. Newborns are screened through a routine blood test. Confirmatory testing (like hemoglobin electrophoresis) or prenatal tests can diagnose it before birth in high-risk families.
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Yes, it’s called Sickle Cell Trait. If you carry one sickle gene, you usually don’t show symptoms but can pass it to your child. Knowing your status helps in planning for the future.
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