Amniochrome Test

The "Amniochrome" test is a highly sensitive and comprehensive prenatal genetic testing panel with clinical utility in detecting subtle and cryptic microdeletions and duplications in the fetus through advanced techniques like Chromosomal Array Comparative Genomic Hybridization (Array CGH), Karyotyping using G-Banding, and Fluorescence In Situ Hybridization (FISH) for specific chromosomes (13, 18, 21, X, and Y). This test is performed using amniotic fluid samples collected during pregnancy and requires maternal blood samples for maternal cell contamination (MCC) studies. The test is essential in identifying potential genetic conditions in the fetus and enables genetic counselors to provide detailed consultations based on the results. To ensure the ethical and legal aspects, a detailed clinical history, including the anomaly scan report, and a duly signed consent form as per the PCPNDT (Pre-Conception and Pre-Natal Diagnostic Techniques) regulations must be submitted along with the sample.