Blood Tests

PGT involves screening embryos for genetic abnormalities before transfer. PGT can help identify embryos with a higher likelihood of implantation and reduce the risk of certain genetic conditions.

Analyzes fetal tissue after miscarriage or abortion. It identifies chromosomal abnormalities, genetic causes, or structural issues underlying pregnancy loss. This information helps couples understand potential factors, enabling informed decisions and guiding future reproductive choices and interventions.  

BRCA1/BRCA2 gene sequencing identifies mutations linked to breast and ovarian cancers. Testing assesses genetic risk, aiding personalized screening and prevention strategies. Positive results inform decisions about surveillance, prophylactic surgery, and targeted therapies, enhancing early detection and management of hereditary cancer risks.

Amniocentesis is a prenatal diagnostic test involving the removal of a small amount of amniotic fluid from the uterus. It helps detect genetic disorders, neural tube defects, and other fetal conditions. Guiding treatment decisions, it carries a slight risk of complications and is typically performed in the second trimester.

Non-Invasive Prenatal Testing (NIPT) analyzes fetal DNA from maternal blood to screen for chromosomal abnormalities like Down syndrome. Safe and accurate, NIPT provides early insight into the baby’s health without invasive procedures, aiding informed decisions and guiding further diagnostic steps if needed. We are the only center in Nepal which has in house NIPT test […]

When it comes to advanced fertility care, understanding genetic health is key to success. Karyotyping, a sophisticated genetic testing process, plays an essential role in diagnosing potential chromosomal issues, especially for those pursuing in vitro fertilization (IVF). At Slavica IVF & Research Center, recognized as the best IVF center in Nepal, karyotyping is an integral […]