Faq
Genetic counselling is a personalised approach that helps individuals and their families understand how genetic factors can contribute to inherited disorders. A genetic counselling programme involves detailed discussion with a team of expert geneticists who provide information about genetic risks, available testing options, interpretation of results, and guidance on managing these conditions.
You should gather all important information relating to you and your family members’ medical histories (including family members—parents, siblings, aunts, uncles, grandparents, and cousins). Organise all records and send them over email to helixgenomix@gmail.com or support@helixgenomix.com 24-48 hours before the counselling session. You can also bring a support person during the session.
Expert geneticists effectively assess familial or individual risks for inherited conditions. They also offer guidance, support, and education about genetic testing and its implications.
Genetic counselling helps to identify genetic risks, make informed choices about testing, and interpret results, aiding in medical management.
Any individual concerned about inherited conditions or who has a personal or family history of genetic disorders can opt for genetic counselling.
No, it’s a personal decision. Geneticists can discuss the benefits, limitations, and implications. However, the final decision about conducting genetic testing stays with that individual.
Yes, geneticists always follow strict confidentiality guidelines to safeguard information. Additionally, under HIPAA, Helix Genomix has certain rights to use your data to provide care and for research purposes. Our team may also contact you for the purposes of clinical trials, treatments, or products that may be relevant to your health condition.