Sickle Cell Disease and Thalassemia are inherited blood disorders that affect the production and function of hemoglobin, the protein responsible for carrying oxygen throughout the body. Early diagnosis helps individuals and families make informed healthcare and reproductive decisions.
At RaktGen Works, we offer advanced testing to identify whether you are a carrier, affected individual, or free from these genetic conditions.
A CBC is often the first screening test and helps evaluate:
These specialized tests accurately identify different types of hemoglobin and help diagnose:
Genetic analysis detects the specific gene mutations responsible for sickle cell disease and thalassemia, providing definitive confirmation and carrier status information.
Testing helps determine whether both partners are carriers and assesses the risk of passing the condition to future children.
Early diagnosis allows timely medical care and improved long-term health outcomes.
Carrier testing can help couples understand genetic risks before starting a family.
Testing may be recommended if you experience: Chronic fatigue , Unexplained anemia , Frequent weakness, Severe joint or abdominal pain, Family history of blood disorders
Sample Type: Blood
FF 14, Swastik Chambar, Income Tax, Ashram Road , Ahmedabad 380014
✔ Early and accurate diagnosis
✔ Carrier status identification
✔ Informed family planning decisions
✔ Better disease management and treatment planning
✔ Support for prenatal and newborn screening