View allAll Photos Tagged GeneticScreening
For patients who are pregnant, the NIPT is a simple, safe and noninvasive way to screen for common chromosomal conditions.
When you’re expecting a baby, you need clear answers about their health, not advice. Non invasive prenatal genetic screening and fetal chromosome DNA tests, were developed to detect any genetic mutations or defects which could lead to developmental problems.
When you’re expecting a baby, you need clear answers about their health, not advice. Non invasive prenatal genetic screening and fetal chromosome DNA tests, were developed to detect any genetic mutations or defects which could lead to developmental problems.
If your patients are undergoing IVF, you can help increase their chances of conceiving with implantation genetic screening
Thalassemia (Congenital Hemolytic Anemia) Testing in Da Nang
“Thalassemia testing is designed to identify both gene carriers and affected individuals across varying degrees of severity. This facilitates informed family planning decisions and improves treatment prognosis.”
What is Thalassemia?
According to the National Institute of Hematology and Blood Transfusion (NIHBT), as of 2017, Vietnam had approximately 12 million Thalassemia gene carriers (15% of the population). More than 20,000 individuals require lifelong treatment, and around 8,000 children are born with the disease each year.
Early screening helps detect carriers before marriage or pregnancy, prevents transmission to future generations, and supports timely medical intervention. This test is essential for couples preparing for marriage, pregnant women, and individuals with a family history of blood disorders.
🔗 Learn more: phongkhammedic.com/thalassemia-congenital-hemolytic-anemi...
📍 Medic Saigon Diagnostic Clinic – 97 Hai Phong Street, Da Nang
📞 Hotline/Zalo: 0914 496 516
#Thalassemia #GeneticScreening #BloodDisorders #PrenatalTesting #MedicSaigon #DaNang #HealthCheck #ThalassemiaTest
Women who are expecting a baby should consider prenatal DNA testing to determine the chances of their babies being born with a common chromosomal condition.