Genetic Screening
- Flagstone Family Practice
- Jul 11
- 2 min read
Supporting Your Health Through Personalised Genetic Risk Assessment
Genetic Screening at Flagstone Family Practice
Genetic screening can provide valuable insights into your inherited risk of certain medical conditions, helping you make informed decisions about your health and your family's future. By identifying genetic predispositions early, you may be able to reduce your risk of disease through appropriate monitoring, lifestyle changes, and preventive care.
At Flagstone Family Practice, our experienced GPs provide personalised genetic risk assessments and coordinate referrals for appropriate genetic testing and specialist care when needed. We are committed to helping individuals and families understand their genetic health with compassionate, evidence-based support.
Who Should Consider Genetic Screening?
Genetic screening may be recommended for people who:
Have a family history of inherited medical conditions
Are planning a pregnancy or starting a family
Have a family history of breast, ovarian, bowel, or other hereditary cancers
Have a personal or family history of inherited heart conditions
Have unexplained medical conditions that may have a genetic cause
Want to better understand their inherited health risks
Genetic Screening Throughout Life
Before Pregnancy
Carrier screening helps identify whether prospective parents carry inherited conditions that could be passed on to their children.
During Pregnancy
Prenatal screening may detect certain inherited or chromosomal conditions, allowing families to make informed healthcare decisions.
Adulthood
Genetic testing can help identify inherited risks for certain cancers, cardiovascular disease, and other chronic conditions, supporting early detection and prevention.
Later in Life
Genetic screening may assist in assessing the risk of some neurological and inherited conditions, helping guide long-term health planning and management.
Genetic Screening Services Available
Depending on your medical history and family history, your GP may recommend testing for:
Carrier Screening
Including inherited conditions such as:
Cystic Fibrosis (CF)
Spinal Muscular Atrophy (SMA)
Fragile X Syndrome
Thalassaemia
Sickle Cell Disease
Hereditary Cancer Screening
Assessment for inherited cancer syndromes, including:
BRCA1 & BRCA2
Lynch Syndrome
Cardiovascular Genetic Testing
Screening for inherited heart conditions, including:
Familial Hypercholesterolaemia
Hypertrophic Cardiomyopathy
Pharmacogenomic Testing
Helps determine how your genes may influence your response to certain medications, supporting safer and more personalised treatment.
Prenatal & Newborn Genetic Screening
Testing available during pregnancy and after birth to identify certain inherited or genetic conditions.
Rare Disease & Neurological Screening
Assessment for selected inherited neurological and rare genetic disorders where clinically appropriate.
How Flagstone Family Practice Can Help
Our experienced GPs provide personalised care throughout your genetic screening journey.
Our services include:
Comprehensive family history and genetic risk assessments
Guidance on appropriate genetic testing
Preconception and reproductive health counselling
Referrals to genetic counsellors and medical specialists
Coordination of specialist investigations and follow-up care
Personalised preventive health plans based on your results
Ongoing monitoring and support
Make Informed Decisions About Your Health
Understanding your genetic health can help you take proactive steps to protect yourself and your family. Whether you're planning a pregnancy, concerned about your family history, or looking to better understand your personal health risks, our team is here to support you.
Book an appointment at Flagstone Family Practice to discuss whether genetic screening is right for you and receive personalised advice tailored to your health needs.
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