Prenatal screening includes blood tests which are done starting at 11 weeks of pregnancy. They apprise you of your chance of having a baby with certain disorders or genetic conditions.
Newborn screening is the practice of testing every newborn for certain harmful or potentially fatal disorders that aren’t otherwise apparent at birth
Cytogenetic tests are confirmatory tests where the structural and number of chromosomes are observed
MKT or Molecular Karyotyping is a revolutionary new technology for analysis of chromosomes
At Lilac Insights, clinical data of every patient adds up to our knowledge repository and helps improve our clinical expertise
Genetic counsellors are health professionals with thorough experience in the field of medical genetics and counselling