New Born Screening is a test to screen a newly born baby within 24-72 hours of birth. It identifies if the new born baby has an IEM disorder (Inborn error of metabolism), that were not observable at the time of birth. These disorders are manageable if identified at an early stage in life. Newborn screening […]
Genetic Screening Test for NBS Cystic Fibrosis – Genes2Me Read More »
Noninvasive Prenatal Screening (NIPS): An innovative approach to understand prenatal genetic disorders and chromosomal abnormalities Noninvasive prenatal diagnostic procedures have revolutionized the diagnostics field to screen rare genetic diseases and chromosomal abnormalities. NIPT; noninvasive prenatal test offered by several diagnostic companies to understand and identify genetic disorders due to chromosomal trisomy. This procedure can be
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