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.
What types of gene testing does BNH offer?
BNH offers varieties of in-depth analysis at the genetic level for Individualized health and disease prevention plans .
SPOT-MAS PACKAGE – Genetic Screening for 10 Types of Cancer
With SPOT-MAS technology, multi-cancer screening is made possible through just a single blood test. This allows you to monitor your health and cancer risks with peace of mind, and provides an excellent option as part of your annual proactive health check.
- The price includes the doctor’s interpretation fee and hospital service charges, but excludes any additional expenses that may arise from further diagnostic examinations or treatments if abnormalities are detected.
- The hospital reserves the right to amend the programme price as appropriate without prior notice.
The Hereditary Cancer Gene Panel is an in-depth genetic test designed to identify inherited cancer risks that may have been silently passed down within your family. It helps you to understand your personal risk, enabling you to plan preventative measures and manage your health in the most precise and effective way – before the disease develops.
This is a test that analyses gene groups associated with hereditary heart disease and high blood cholesterol.
This is a Stool DNA Test, which analyses the DNA of cancer cells from a stool sample. It is a convenient and highly accurate method that enables the detection of risks at an early stage. The test is suitable for annual screening or as an alternative to colonoscopy at regular intervals.
It is a genetic test designed to personalise cardiovascular treatment, helping to determine which medications are most effective for your body and which may pose a higher risk of adverse reactions.
This test analyses fundamental genes related to nutrition to help you understand how your body responds to nutrients, vitamins, and minerals. It creates a personalised nutrition guide based on your genetic information.
This is an advanced and comprehensive genetic test that provides in-depth insights—not only into your response to nutrients, but also your metabolic potential, tendencies for fat accumulation, response to different types of exercise, and genetic risks for non-communicable diseases (NCDs).
ทำนัดหมายแพทย์
– อายุรกรรมทั่วไป
– 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
ตารางออกตรวจแพทย์
| วัน | เวลา | แผนก |
|---|---|---|
| อังคาร | 08:00 – 12:00 | ศูนย์ตรวจสุขภาพ |
| พุธ | 08:00 – 12:00 | ศูนย์ตรวจสุขภาพ |
| พฤหัสบดี | 08:00 – 12:00 | ศูนย์ตรวจสุขภาพ |
| ศุกร์ | 08:00 – 13:00 | ศูนย์ตรวจสุขภาพ |
