Genetic Counselling
Guiding You with Care: Personalized Genetic Counselling for a Healthier Future
Reasons to Undergo Genetic Testing
There are many reasons prospective parents may consider genetic testing, and the choice depends on individual circumstances. Below are some common reasons people choose this option:
- Family History: If there are birth defects or hereditary conditions in your family, genetic testing can help evaluate risks for your future children.
- Challenges in Previous Pregnancies: If you’ve experienced infertility, multiple miscarriages, or had a child with a birth defect, genetic testing may provide useful insights.
- Family Cancer History: If there’s a history of recurring or early-onset cancer, testing can help evaluate hereditary risks.
- Age-Related Factors: Genetic testing can assess increased risks due to advanced parental age (mother over 35 or father over 45).
- Abnormal Test Results: If you’ve received positive ultrasound results or other pregnancy tests, additional genetic testing can provide more detailed information.
- Exposure to Environmental Factors: If you’ve been exposed to certain medications, radiation, or infections during pregnancy, genetic testing can evaluate potential impacts.
How is Genetic Testing Performed?
Genetic testing is a careful and personalized process. It begins with a meeting with our clinical geneticist, who will discuss your health and gather detailed information about your family’s medical history. Together, you will create a family tree covering at least three generations to identify patterns or hereditary conditions that may be present.
Based on this family history, the geneticist may recommend specific tests or consultations with other specialists. These may include:
Throughout this process, we’re here to support you with clear explanations and compassionate care. Our goal is to ensure you feel informed and comfortable, providing the knowledge needed to make the best decisions for your family’s future.
- Chromosomal Analysis (Karyotype Study): To check for chromosomal abnormalities that could affect fertility or the baby’s health.
- Genetic Mutation Testing (Carrier Screening): To look for specific gene changes that could be passed to your children.
- Ultrasound: To gain a clearer picture of the baby’s development.
- Other Necessary Tests: Any additional evaluations that may provide insight into your genetic health.
Costs of Genetic Counselling
Understanding the costs of genetic counselling can help you plan with confidence. Expenses vary depending on the specific tests and level of analysis required. Some costs may be covered by insurance, especially if there is a known genetic risk or a family history involved.
For detailed pricing information, please refer to our price list.
Genetic Counselling
FAQs
Who should consider genetic counselling?
Genetic counselling can benefit anyone planning to start or expand their family, particularly those with a family history of genetic disorders, complications in previous pregnancies, recurrent miscarriages, or advanced parental age. It is also helpful for those exposed to certain environmental factors or those seeking more information about their genetic health.
What can I expect during a genetic counselling session?
During the session, you’ll meet with a genetic counsellor who will review your medical and family history in detail. They’ll discuss potential genetic risks, answer your questions, and help you understand your testing options and next steps. The goal is to provide the information you need to make informed decisions.
What types of genetic tests are available?
There are several types of genetic tests that may be recommended, such as chromosomal analysis, genetic mutation tests. The specific tests recommended will depend on your individual circumstances, family history, and the information gathered during your counselling session.
How long does the genetic counselling process take?
The length of the process can vary. A typical counselling session lasts about an hour, but the overall process, including recommended tests, may take several weeks. Your genetic counsellor will guide you through each step and provide a timeline based on your specific situation.
What happens if a genetic risk is identified?
If a genetic risk is identified, your counsellor will explain the findings in detail and discuss what they mean for your fertility or pregnancy. They’ll also outline your options and next steps, which may include additional testing, treatments, or referrals to specialists. The goal is to provide all the information and support you need to make informed decisions.
Can genetic counselling help with fertility treatments?
Yes, genetic counselling can play a crucial role in fertility treatments. Understanding your genetic health can help identify potential risks or challenges early on, enabling you and your healthcare provider to tailor your treatment plan for the best possible outcome.
Is genetic counselling confidential?
Absolutely. Genetic counselling is a confidential process. All information discussed during your sessions and test results is kept private and shared only with your consent.
How should I prepare for a genetic counselling appointment?
To make the most of your session, it’s helpful to gather information about your family’s medical history, including known genetic disorders, birth defects, or disease patterns. Bringing this information to your appointment can help your counsellor provide a more comprehensive assessment.