Preventive Genomics and Integrative Medicine

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‘Prevention is better than cure’ is a phrase commonly used by doctors, nurses and even mums and dads. There can be no doubt that it is better to stop an illness from occurring than it is to treat it after it has happened. But how is it possible to know you have chance of suffering a specific illness before it occurs?

Thanks to developments in Genomic Medicine it is now possible to look at each individual’s genetic code to help us understand the risk of developing various diseases and plan how we can avoid contracting disease. 

Angeline Jolie, whose mother died of breast cancer when she was 56, brought global attention to genetic testing in 2013 after undergoing test to find out her own risk of developing the disease. Her estimated lifetime risk of breast cancer was 87%, prompting her to undergo a preventive double mastectomy to reduce her risk of breast cancer to closer to 5%.

How genes impact our lives
Our genes make us unique, but they also give insights into your health history. This is important when identifying serious diseases like cancer, heart disease, and other genetic diseases as these are passed through family genes. 

Understanding more about your risk of serious diseases can help you prepare disease prevention.

What is gene testing?
Traditional medical examinations are based on looking at patient history, symptoms, and lab tests. Genetic testing identifies changes in your DNA by analyzing your cells or tissue to look for any changes. This is commonly done by taking a blood or cheek swab sample, although samples may be taken from hair, saliva, skin, or in the case of pregnant women, amniotic fluid. Samples can be taken at home, or at the hospital.

Samples are then sent to the lab for testing and analysis by skilled medical geneticists, followed by a counselling session between the patient and the medical geneticist to discuss test results.

What are the benefits of gene testing? 
Genetic testing gives accurate and reliable information to doctors to help them make recommendations for treatment or monitoring.

The main benefits of genetic testing are to :
  • Predict future health and enable proper planning to prevent certain serious diseases.
  • Reduce the risk of drug allergy and help predict drug response to inform appropriate drug choice and dosage
  • Guide family planning decisions by detecting certain hereditary diseases and conditions
Understanding your genes can help everyone understand their and their families’ health. 

Common groups that undertake genetic testing
Couples who are thinking about starting a family – genetic testing can :
  • discover if the prospective parents are carrying genes that could pass diseases to their children 
  • lower the risk of genetic diseases in embryos created using assisted reproductive technology 
  • screen new babies for certain diseases
  • find genetic diseases in unborn babies 
Anyone who cares about their health, or has a family history of inherited diseases
  • diagnose diseases such as heart disease, cancer, diabetes and others
  • identify genetic changes to a disease you have already been diagnosed with
  • understand how severe a disease may become
  • help your doctor understand which medicine and dosage is best for you, and which isn’t good for you

Gene testing services at Bumrungrad
At Bumrungrad each test is processed at our world-class accredited hospital lab. After this a genetic medicine specialist can accurately interpret the results, and specialists in all related fields are ready to provide advice on health care and holistic treatment.

At Bumrungrad, we use Next-Generation Sequencing (NGS) technology to analyse the decoding of many genes at the same time. This process is fast and accurate, allowing physicians to quickly use the results of the tests to assess the risk of serious diseases and analyse other diseases now, and in the future. 

Preventive Genomics and Integrative Medicine Center offers a comprehensive range of services from diagnosis, consultation, disease screening and risk assessment for inherited diseases and pharmacogenetic testing for drug selection, dose adjustment, and drug allergy prevention. The services are available for people with a family history of hereditary diseases and for individuals who care about their own and their families’ health.



Bumrungrad offers the following genetic testing services to assess the risk of diseases:


Related Health Blogs:

Genetic disorders
Genetic disorders are caused by changes in the DNA sequence, partial or whole, resulting in abnormal DNA sequences. They may be caused by a variation in a single gene (monogenic disorder), by mutations in multiple genes (multifactorial inheritance disorder), by a combination of gene mutations and environmental factors, or by damage to chromosomes.
With the rapidly progressing field of genetics and genomics, we now know that genetics is a major factor affecting health. Some diseases may be caused by genetic mutations or germline mutations, passed on to offspring, such as cystic fibrosis and certain cancers. On the other hand, several cancers result from somatic mutations, of which causes include exposure to toxic environments, certain viral infections and aging.
Common genetic disorders
There are several types of genetic disorders depending on the genetic material abnormality. But common ones are the following:

  • Polycystic kidney disease is caused by the defect in the PKD1 gene, causing the patient to have a large number of cysts in the kidneys, which increases over time. The cysts of different sizes may spread all over the kidneys, reducing renal function, developing into chronic kidney disease in the late stages, then kidney failure and death. It also causes complications such as high blood pressure, gallstones, and infections. Those with hereditary PKD may show no symptoms for decades and then begin to develop symptoms in their 30-40s.

  • Sickle cell disease is caused by mutation in genes, causing a red blood cell disorder, making the cells of sickle shape, unhealthy, short-lived and break apart easily. This leads to anemia and also causes arm pain, swollen feet, and life-threatening complications such as liver failure, pulmonary hypertension, and cerebrovascular disease.

  • Cystic fibrosis is a genetic condition caused by a mutation in CFTR gene The body thus produces thick and sticky mucus, clogging the lungs, which can lead to difficulty breathing and severe lung infections. The sticky mucus also blocks the secretion of enzymes used to digest food in the pancreas, causing problems with the digestive system and then a lack of key nutrients. The mucus also clogs the ducts connecting the testicles to the prostate resulting in male infertility. Women with cystic fibrosis will find it difficult to get pregnant.

  • Huntington's disease is caused by a mutation in the Huntington gene and its production of abnormal proteins, resulting in the degeneration of nerve cells in the brain, and in turn, movement, cognitive, and psychiatric disorders. Functional abilities keep worsening until the person finds it hard to move or self-care and suffers from dementia. Risks of complications include heart disease, pneumonia and falls. Patients usually die within 20 years of the onset of symptoms.

  • Thalassemia is a type of anemia caused when the body makes an abnormal form or inadequate amount of hemoglobin in red blood cells. A person with Thalassemia usually has pale or yellowish skin and in mild cases, can lead a normal life. But in severe cases, the person may suffer from facial bone deformities, slow growth, enlarged liver and spleen, vulnerability to infection, and brittle bones.

  • Hemophilia is a malfunction of the genes affecting the coagulation factors, causing easy bleeding, which is then hard to stop. It is a disorder found only in men as women who is a carrier of the hemophilia gene are asymptomatic. Symptoms vary depending on the severity of the disease. In mild cases, heavy bleeding may occur only after an accident, a surgery or a tooth extraction, when the bleeding is found hard to stop. In severe cases, the patient has bruises all over the body, bleeding in the muscles and joints, and possibly bleeding in other organs such as the gastrointestinal tract and the brain.

  • Down syndrome is condition in which a child is born with an extra full or partial copy of their 21st chromosome, causing physical and mental developmental delays. Common physical characteristics include a flat facial feature, bulging tongue, small head and ears, upward slanting eyes, short neck, round face, plus short and wide hands. Children with Down syndrome are short and tend to be overweighed growing up. Complications include congenital heart disease, thyroid disease, hearing loss, cataract and dementia as well as vulnerability to infections. Risks of giving birth to a child with Down syndrome include the expecting mother being over 35, the mother previously having a child with Down syndrome, or with a family history of Down syndrome.

  • Color blindness (Color vision deficiency) is the decreased ability to see color or differences in color.  The most common cause of color blindness is a genetic disorder in the development of one or more of the three sets of the eyes' cone cells, which sense color. These cone cells sense wavelengths of light and enable the retina to distinguish between colors. Abnormal photoreceptor cells thus cause impaired color vision. Most patients cannot distinguish between red and green. In severe cases, the patients may see things only as black and white or in shades of gray.

Cancer risk
Cancer is caused by mutations in genes, accelerating cell division rates or inhibiting normal controls on the cell cycle. Gene mutations can be spontaneous or triggered by environmental pollution or exposure to carcinogens. Gene mutations can also be inherited from parents to offspring. When transmitted to a child, a germline mutation is incorporated in every cell of the body. Common genetically inherited cancers include breast cancer, uterine cancer, retinoblastoma, pancreatic cancer, ovarian cancer, colorectal cancer, prostate cancer and thyroid cancer.

Familial hypercholesterolemia

Hypercholesterolemia is caused by certain genetic mutations that limit the body’s ability to remove LDL cholesterol from the blood, the most common being a mutation in the LDL receptor gene. In addition, bad cholesterol can accumulate in various organs throughout the body, and if this happens in the coronary arteries, it can lead to coronary artery disease or an atheroma, which puts those with familial hypercholesterolemia at risk for developing heart disease at an early age

Inborn errors of metabolism

A group of genetic diseases comprising over 700 diseases that cause death or severe disability in infants and frequently recur in families because faulty gene is hidden within families/ parents. These inborn errors of metabolisms lead to an inability of protein or enzyme production that interfere breakdown of different substances in the body. Therefore, different organs are affected.

Cardiovascular risk
Genes regulate many aspects of the cardiovascular functions. Cardiovascular diseases can ensue from a gene mutation.  Several of such diseases can be inherited, including arrhythmias, congenital heart disease, hypertrophic cardiomyopathy (HCM), idiopathic dilated cardiomyopathy (DCM), hyperlipidemia, coronary artery disease, and heart failure. Thus, in a family where a member has a heart disease especially at a young age or sudden death, other family members are recommended to be tested for the risk of developing a heart disease even without any symptoms.

Drug allergy risk
Different people respond differently to a drug. Some drugs may be more effective in one person than in another. Also, some people may have an overreaction to the drug, known as a drug allergy. Symptoms range from mild to moderate including rash, swelling, fever, to severe allergic reactions which could result in abnormal and life-threatening conditions such as bronchospasm, causing difficulty breathing, swollen tongue blocking airway, diarrhea, low blood pressure, seizures and loss of awareness, etc. Genetic testing allows doctors to choose the most appropriate drugs for the patient so as to avoid drug allergy. This further helps save treatment time and cost as appropriate drugs can be prescribed right from the start without trial and error.


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Dr. Chanin Limwongse


Internal Medicine - Medical Genetics
Pathology (Clinical Pathology)

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Dr. Prasit Phowthongkum


Internal Medicine
Internal Medicine - Medical Genetics

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Asst.Prof.Dr. Polakit Teekakirikul


Cardiology - Cardiac Genetic
Internal Medicine - Medical Genetics

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Col.Asst.Prof.Dr. Kitti Buranawuti


Internal Medicine - Medical Genetics

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Dr. Tim Phetthong


Pediatrics - General Pediatrics
Pediatrics - Pediatric Genetics

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Dr. Nithiwat Vatanavicharn


Pediatrics - Pediatric Genetics

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Dr. Janewit Wongboonsin


Internal Medicine - Medical Genetics
Internal Medicine - Nephrology

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  • Preventive Genomics and Integrative Medicine 
    Service Hours: Monday through Sunday 8:00 am to 6:00 pm 
  • Service hours for centers/clinics may change without prior notice due to safety protocols put in place to prevent the spread of COVID-19. As a result, we ask that you please schedule your appointments in advance or call to recheck service hours before travelling to the hospital. Tel. 1378 (local calls only)


  • Preventive Genomics and Integrative Medicine 
    Location: Preventive Genomics and Integrative Medicine  : Building B, 3rd floor
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