Precision Medicine "The KEY to Healthy Longevity"
Also known as Personalised Medicine, an innovative approach to tailoring disease prevention and treatment that takes into account differences in people's genes, environments, and lifestyles.
The goal is to target the right treatments to the right patients at the right time.
Genomics Screening
The powerful discoveries treatments that are tailored to specific characteristics of individuals.
A person's genetic information has the ability to transform the way medicine is practiced, making what once seemed impossible possible.
What is genetic testing?
Genetic testing is a type of medical test that identifies specific inherited changes (mutations) in chromosomes, genes, or proteins. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder.
Why Get Genetic Testing?
An in-depth health assessment for personalized screening and preventive healthcare plan. Genetic testing is a powerful tool to identify those individuals who are at increased lifetime risk for developing certain diseases, find if you have genes that may increase cancer risk for your children. It allows you and your doctor to create a personalised care plan to prevent or detect certain diseases at an earlier or more treatable stage.
Who should consider Genetic Testing?
The Test is for anyone who wants to understand about their genetic insights, to discover how genetics can impact your likelihood of developing certain health conditions or having certain traits; especially in these groups: • People with a personal or family history of cancer • People and their families with a known family mutation • Couple who plan to start a family • People who are interested in learning more about their genetics
When Should You Consider Genetic Testing?
The test can be done in all adults who are looking for the better health prevention in their lifetime healthcare plans. It is highly recommended if you have a family history of a genetic disorder or symptoms of a disease that may be caused by genetic changes. As everyone has a unique genome, this complex once-in-a-lifetime test can help identify genetic variants that may relate to your health.
How to do the test?
Genetic Cancer Screening, using 3 ml. blood collection. Cutting-edge lab technology provides results with accuracy >99%. Thus this valuable information can help you and your family plan for preventive measures long before the condition presents. It also provides the best treatment success chances available.
Where is the Genetic screening available?
BNH Hospital Genomic Medicine offers intuitive and efficient ways of managing and delivering care at the important points along your health journey. By leveraging the latest medical, genomic and technological advancements together with our genomics specialists and multidisciplinary team of healthcare providers, we are able to address and help to solve your difficult healthcare challenges. Your health data are strictly protected with our Data Protection Privacy Policy.
GENOMICS SCREENING at BNH Hospital
BNH offers varieties of in-depth analysis at the genetic level for Individualized health and disease prevention plans .
A proactive health screening that predicts the risk for certain cancers due to inherited genetic mutations in order to plan personalised medical interventions and preventive measures.
Genetic testing for individual nutrient assessment, food response, metabolism, taste sensitivity, absorption of vitamins as a guideline for health planning; foods, nutrient and vitamin supplementation, and effective exercise.
Evaluate individual drug response and efficacy, drug allergy risk, to reduce the likelihood of side effects and drug allergies, helping doctors select the most effective drugs and minimize adverse drug reactions.
Colorectal Cancer Panel analyzes genes associated with a hereditary predisposition to colorectal cancer. Genetic testing of these gene allows for accurate risk assessment and more precise screening approaches to prevent the development of colorectal cancer.
Breast and Gynecologic Cancers Panel analyzes genes that are associated with hereditary predisposition breast, ovarian, and endometrial/uterine cancers, in order to allows more precise identification of those who are at an increased risk of inherited breast cancer and gynecologic cancer.
Determine the risk of having an inherited gene mutation that increases the risk of breast and ovarian cancers
Genetic Breast Cancer Screening Panel analyzes genes that are associated with hereditary predisposition to breast cancer which may help confirm a clinical diagnosis, help predict disease prognosis and progression, facilitate early detection of symptoms, and inform family planning and genetic counseling.
Exome sequencing for cardiovascular disease + Pharmacogenomics | การตรวจยีนเพื่อค้นหาความเสี่ยงโรคหัวใจ + การตรวจยีนทางเภสัชพันธุศาสตร์ (ตรวจยีนแพ้ยาและการตอบสนองต่อยา)
Contact us to inquire or make an appointment.
Appointment
Pornpimol Srisuphonvanij, M.D.
Advance Diagnostic Centre (Check-up), Internal Medicine
Specialty
Internal Medicine
Language
Thai, English
– Diplomate, Thai Board of Internal Medicine , Ramathibodi Hospital, Mahidol University (2013)
– MD., Ramathibodi Hospital, Mahidol University ,2006
– Residency Training in Internal Medicine, Ramathibodi Hospital, Mahidol University ,2013
Doctor’s Schedule
| Day | Time | Location |
|---|---|---|
| Tuesday | 08:00 – 14:00 | Advance Diagnostic Centre (Check-up), Internal Medicine (BNH All season) |
| Wednesday | 08:00 – 14:00 | Advance Diagnostic Centre (Check-up), Internal Medicine (BNH All season) |
| Thursday | 08:00 – 14:00 | Advance Diagnostic Centre (Check-up), Internal Medicine (Advance Diagnostic centre ( Presicion medicine )) |
| Friday | 08:00 – 14:00 | Advance Diagnostic Centre (Check-up), Internal Medicine (Advance Diagnostic centre) |
Contact us to inquire or make an appointment.
