Mother and Child Healthcare
Complete Genetic solutions to safeguard mother and child health
Non Invasive Prenatal Screening is a simple non-invasive blood test to screen for common genetic abnormalities in developing baby. It is done by analyzing fetal DNA isolated from mother's blood by Next Generation Sequencing. "Crysta-NIPS" offer world class tech for accurate and actionable results.
CRYSTA CARRIER SCREENING
Crysta Carrier Screening Panel covers over ~300 genes that are associated with around 400 disorders inherited in an Autosomal recessive (some X-Linked recessive) manner and are mostly severe childhood onset diseases.
PGS (widely known as aneuploidy screening) involves checking the chromosomes of embryos created by in vitro fertilisation (IVF) or intracytoplasmic sperm injection (ICSI) for abnormalities. PGS gives information about embryos' genetic health to select the best embryo to transfer.