Sickle Cell Disease
An inherited condition where red blood cells become sickle-shaped, causing anaemia, painful episodes and infections.
Quick Summary
Episodes of severe pain, anaemia, tiredness, swelling of hands and feet, frequent infections and yellow eyes.
Pain relief, fluids, hydroxyurea, vaccinations and antibiotics, blood transfusions and specialist care.
Inherited from both parents. Common among some tribal communities in India.
Overview
In sickle cell disease, abnormal haemoglobin makes red blood cells stiff and curved. They block small blood vessels and break down early.
India has a national mission to screen and support people with sickle cell disease. Early diagnosis and care improve life expectancy.
Symptoms
Pain crises
Sudden severe pain in bones, chest or tummy.
Anaemia
Tiredness and breathlessness.
Swollen hands and feet
Especially in young children.
Emergencies
Fever, chest pain, breathing trouble or stroke signs need urgent care.
Causes & Risk Factors
Biological Causes
Inheriting two sickle haemoglobin genes (one from each parent).
Key Risk Factors
- Family history Both parents carrying sickle cell trait.
- Community Higher rates in some tribal populations.
- Triggers for crises Dehydration, cold, infection and stress.
Management & Treatment
01. Prevent crises
Drink plenty of fluids, avoid extreme temperatures, and treat infections early.
02. Hydroxyurea
Reduces pain crises and complications.
03. Preventive care
Vaccines, folic acid, and regular check-ups.
Frequently Asked Questions
Is sickle cell trait a disease?
Can it be cured?
How is it diagnosed?
Sources and further reading
Last updated 21 October 2026. For more detail, see these trusted health organisations.
- Sickle Cell Disease(opens in a new tab) · MedlinePlus, US National Library of Medicine
- Sickle cell disease(opens in a new tab) · NHS