Prenatal sampling procedure that analyzes placental tissue for detecting chromosomal and genetic abnormalities in early pregnancy stages.
Chorionic Villus Sampling (CVS) is a prenatal diagnostic test that examines placental tissue to detect chromosomal or genetic disorders in the developing baby. Performed with precision at Dr. Ashwini’s Scans and Labs, it provides early, accurate insights for families facing high-risk pregnancies.
Chorionic Villus Sampling (CVS) is a specialized prenatal procedure used to diagnose chromosomal and inherited disorders at an early stage of pregnancy—typically between the 10th and 13th weeks. During the procedure, a small tissue sample is collected from the placenta, which shares the baby’s genetic material.
At Dr. Ashwini’s Scans and Labs, CVS is performed under continuous ultrasound guidance by experienced specialists to ensure precision and safety. The collected sample undergoes detailed genetic analysis to detect chromosomal abnormalities such as Down syndrome, Trisomy 18, and other inherited conditions.
This procedure is recommended for women with abnormal screening results, family history of genetic disorders, or pregnancies identified as high-risk due to maternal age or prior outcomes.
By offering accurate, early insights into the baby’s genetic health, CVS enables timely counseling and informed medical decisions. The facility maintains strict sterility protocols and uses state-of-the-art equipment to minimize risks and ensure optimal outcomes.
Comprehensive pre-procedure counseling is provided to address parental concerns and explain potential implications. Post-procedure monitoring ensures maternal and fetal well-being throughout the diagnostic process. Dr. Ashwini’s Scans and Labs ensures every procedure is conducted with utmost care, patient comfort, and clinical expertise.
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With advanced imaging support and expert prenatal specialists, Dr. Ashwini’s Scans and Labs ensures precise, safe, and early genetic diagnosis through CVS testing.
Ensures accurate sample collection under expert imaging supervision.
Detects a wide range of chromosomal and inherited disorders.
Provides genetic results in the first trimester of pregnancy.
Performed by specialists prioritizing safety, comfort, and clear guidance.
CVS offers expectant parents the opportunity to understand their baby’s genetic health early in pregnancy. It delivers vital information about chromosomal and inherited conditions, helping families make confident and informed choices.
At Dr. Ashwini’s Scans and Labs, the procedure is performed in a sterile, patient-centered environment using continuous ultrasound guidance for maximum accuracy and safety. Genetic analysis is carried out in collaboration with expert cytogenetic and molecular specialists to ensure reliable interpretation.
CVS is typically advised when initial screening results show abnormal findings or when there’s a family history of genetic disorders. Results help doctors and parents plan further diagnostic steps or pregnancy management options.
Known across Bangalore for precision-driven prenatal care, Dr. Ashwini’s Scans and Labs combines advanced technology with compassionate expertise, supporting families through every stage of their diagnostic journey.
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