Genetic counselling plays an important role in helping expectant parents understand potential genetic conditions that may affect their baby. During pregnancy, certain screening tests or ultrasound findings may raise questions about inherited conditions or chromosomal abnormalities. Genetic counselling provides clear medical guidance so families can make informed decisions about their pregnancy and available diagnostic options.
At Fetal View Sonography Centre, genetic counselling is provided as part of a comprehensive fetal medicine approach. The goal is to explain test results, discuss possible risks, and guide families through further screening or diagnostic procedures when required.
Genetic counselling sessions focus on understanding family history, interpreting prenatal screening results, and discussing the benefits and limitations of additional tests such as amniocentesis or chorionic villus sampling (CVS). By providing clear explanations and compassionate support, parents can better understand the next steps in their pregnancy journey.
Genetic information can sometimes feel overwhelming for families. Professional counselling helps simplify complex medical information so parents can understand their options and make decisions with confidence.
Each counselling session involves reviewing the medical history of the mother, father, and family members. This helps evaluate whether there may be an increased risk of inherited or chromosomal conditions.
Many antenatal scans and blood tests are designed to screen for certain conditions during pregnancy. Genetic counselling helps interpret these results and explains whether further evaluation or testing may be recommended.
"Understanding genetic risks during pregnancy can feel overwhelming for many families. Genetic counselling helps parents interpret screening results, understand possible genetic conditions, and explore appropriate diagnostic options. With expert guidance and clear explanations, expectant parents can make informed decisions with confidence throughout their pregnancy journey."
Genetic counselling is often advised in situations where additional guidance can help evaluate potential risks or clarify screening results.
If there is a known history of inherited conditions in the family, counselling helps assess possible risks for the baby and discuss available testing options.
Certain prenatal screening tests or ultrasound findings may suggest a higher probability of chromosomal abnormalities. Genetic counselling helps explain what these results mean and what further tests may be considered.
Women who become pregnant at an older maternal age may have a slightly higher chance of chromosomal abnormalities. Counselling helps families understand screening and diagnostic options available during pregnancy.
If a previous pregnancy was affected by a genetic or chromosomal condition, counselling provides guidance about recurrence risks and preventive monitoring.
Genetic counselling also involves discussing the diagnostic tests that may be recommended when more detailed evaluation is required.
CVS is an early pregnancy diagnostic procedure that examines placental tissue to detect certain chromosomal or genetic conditions.
Amniocentesis involves testing a sample of amniotic fluid to identify chromosomal abnormalities or specific genetic disorders in the baby.
These procedures are only recommended when medically necessary and are performed after detailed counselling to ensure parents fully understand the benefits, risks, and purpose of the test.
Genetic counselling is a step-by-step process designed to provide clarity, reassurance, and expert medical guidance.
The session begins with a detailed discussion about family medical history, previous pregnancies, and screening results.
The doctor explains the possible genetic risks and helps parents understand what the results of screening tests may indicate.
If required, diagnostic procedures such as amniocentesis or CVS may be discussed to confirm certain conditions.
Genetic counselling is not only about medical evaluation—it also focuses on providing emotional support and clear communication for expecting parents.
Families often have many questions after screening tests or ultrasound findings. Genetic counselling ensures that parents receive accurate information, realistic expectations, and compassionate guidance throughout the pregnancy.
At Fetal View Sonography Centre, counselling sessions are conducted by Dr. Pranita Mahashabde, a fetal medicine specialist with advanced training in prenatal diagnosis. Her approach focuses on helping families understand complex medical information in a simple and reassuring way while ensuring the best possible care for both mother and baby.
All scans are performed under the supervision of Dr. Pranita Mahashabde, a fetal medicine specialist with advanced expertise in prenatal diagnosis, ensuring accurate evaluation and compassionate care for every pregnancy.
Genetic counselling during pregnancy is a medical consultation that helps expectant parents understand the possibility of genetic or chromosomal conditions in the baby. During the session, a fetal medicine specialist reviews family history, prenatal screening results, and ultrasound findings to evaluate potential risks. The purpose of prenatal genetic counselling is to help parents clearly understand what the results mean, whether additional testing may be recommended, and what options are available. This guidance helps families make informed decisions about their pregnancy while reducing confusion and anxiety related to genetic testing.
Genetic counselling may be recommended in several situations during pregnancy. It is commonly advised when screening tests indicate a higher risk of chromosomal abnormalities, when ultrasound scans show findings that require further evaluation, or when there is a known family history of inherited conditions. It may also be suggested for women of advanced maternal age or for couples who previously had a pregnancy affected by a genetic disorder. In such situations, genetic counselling helps parents understand the possible risks and discuss whether diagnostic tests such as amniocentesis or chorionic villus sampling (CVS) are appropriate.
During a genetic counselling session, the doctor first gathers detailed information about the medical history of both parents and their families. Previous pregnancies, prenatal screening reports, and ultrasound findings are also reviewed carefully. The fetal medicine specialist then explains whether there may be an increased risk of certain genetic conditions and what further testing options are available. Parents are given clear information about the purpose, benefits, and limitations of diagnostic procedures so they can make decisions with confidence. The session also provides an opportunity to ask questions and receive reassurance about the pregnancy.
Depending on the pregnancy and screening results, the doctor may discuss different prenatal diagnostic tests. Two commonly recommended procedures are chorionic villus sampling (CVS) and amniocentesis. CVS is usually performed earlier in pregnancy and involves examining placental tissue to detect certain genetic conditions. Amniocentesis involves testing a small sample of amniotic fluid to identify chromosomal abnormalities or specific inherited disorders. These tests are recommended only when medically necessary, and the risks and benefits are explained in detail during genetic counselling.
Expectant parents looking for genetic counselling in Mumbai can consult Dr. Pranita Mahashabde at Fetal View Sonography Centre in Vile Parle West. The clinic provides comprehensive fetal medicine services, including prenatal scans, genetic counselling, and invasive diagnostic procedures under one roof. With advanced training in prenatal diagnosis and extensive experience in fetal medicine, Dr. Pranita Mahashabde helps parents understand complex genetic information and guides them through the next steps in their pregnancy with clarity and compassion.
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