Thalassemia Screening is the process to screen for all the hemoglobinopathies, which means disorders affecting the function of hemoglobin in the blood, to find out if a person (especially a parent) is affected by Thalassemia or is a carrier of Thalassemia. The hemoglobinopathies include Alpha, Beta, Delta Thalassemia, Hemoglobin E, Hemoglobin D, Sickle Cell Anemia, Hereditary Persistence of Fetal Hemoglobin (HPFH). Ingin melihat data talasemia anda? Lihat Disini
The Thalassemia Research Center (TRC) is a foundation committed to creating a better world without Thalassemia.
Our mission is to educate people at all levels of society about Thalassemia, to become the world’s most comprehensive Thalassemia screening center and database, to serve as a research and production hub for pharmaceutical preparations for Thalassemia patients, and to advocate for global Thalassemia policies.
Williamsburg occupy sustainable snackwave gochujang. Pinterest cornhole brunch, slow-carb neutra irony.
Williamsburg occupy sustainable snackwave gochujang. Pinterest cornhole brunch, slow-carb neutra irony.
THALASSEMIA SCREENING IS AN ADVANCED GENETIC TEST CONDUCTED ON NORMAL BLOOD SAMPLES THAT HELP TO EVALUATE WHETHER A POTENTIAL PARENT OR AN INDIVIDUAL IS A CARRIER OF THE THALASSEMIA GENE OR IS AFFECTED BY THE DISORDER.
BASED ON THIS INFORMATION, THE COUPLE CAN UNDERGO FURTHER TESTING TO FIND OUT IF THE FETUS IS AFFECTED WITH THE DISEASE, IS A CARRIER OF THE DISEASE OR IS UNAFFECTED. BECAUSE GENETIC DISORDERS ARE NON-TREATABLE, A CHILD AFFECTED WITH B-THALASSEMIA REQUIRES SPECIAL AND EXPENSIVE MEDICAL TREATMENT WITH LOW SURVIVAL RATES. SCREENINGS GIVE PARENTS THE FREEDOM TO MAKE INFORMED DECISIONS CONCERNING THEIR PREGNANCY & FUTURE.
Stay updated with the latest health news and articles. Explore tips, trends, and insights into maintaining a healthy lifestyle.