Transform your health journey with advanced genetic testing services designed for personalized insights and proactive care. At MedEx, we go beyond ordinary testing to provide a comprehensive view of your DNA and its impact on your health and future.
Featured Genetic Tests: DNA Methylation. NIPT/NIPS. Paternity Test. Hereditary Cancer and Carrier Screening. Health Risks Assessment. Pharmacogenetics. Ancestry Insights. Whole Exome Sequencing. Epigenetics. Gut Microbiome.
✅ Comprehensive Testing, Actionable Insights and Expert-Led Consultations
✅ Easy-to-understand Illustrative Reports with Actionable Recommendations Straight to Your Inbox
✅ Secure, Private and Confidential Screening and Proactive Healthcare Solutions
✅ Clinician Assisted Specimen Collection at Network Facilities or at On-Demand Location
✅ Convenient Comprehensive Offerings in One Place, Trusted by 350K+ Patients
GENETIC TESTS CATALOG
✨ DNA Methylation Testing to explore epigenetic markers
🌟 Hereditary Cancer and Carrier Screening for familial health risks
🧬 Health Risks Assessment and Customized Wellness Planning
💊 Pharmacogenetics for medication compatibility
🌍 Ancestry Insights to uncover your genetic heritage
🔬 Whole Exome Sequencing for detailed genetic analysis
🍃 Gut Microbiome Genetic Testing for digestive health insights
👶 NIPT/NIPS Screening for baby's gender and genetic abnormalities
👨👩👧 Pre- and Postnatal Paternity Testing for parental verification
🌸 VISTA Pre-Pregnancy Genetic Testing for planning a healthy family
🤰 NIFTY Fetal Genetic Health Assessment for advanced prenatal care
📜 Genetic Blueprint Testing to unlock your DNA's potential
⚕️ COLOTECT Colon Cancer Screening for early detection
🩺 Genetic Testing for Diseases and Afflictions to identify predispositions
With DNA Methylation Tests of MTHFR, MTR, MTRR, COMT and BHMT Genes
Embark on a transformative journey of self-discovery with DNA Story Premium DNA 500+ Reports Package that also includes Methylation Tests of MTHFR, MTR, MTRR, COMT and BHMT Genes .
--->SAMPLE REPORT ABOVE<---
Unlock over 500 genetic insights, unraveling the mysteries of your health and innate talents. Tailored for all ages, the package empowers you to make informed decisions for a healthier and more fulfilling life. Embrace the power of your DNA with our cutting-edge analysis and embark on a path to optimized well-being and self-awareness. Your DNA Story awaits.
PACKAGE INCLUDES:
1. Methylation Test
Methylation is a fundamental biochemical process that involves the addition of methyl groups to various molecules, including DNA, proteins, and neurotransmitters. Methylation plays a vital role in gene expression, detoxification, energy production, and neurotransmitter balance. A Methylation Test assesses genetic variations that can impact an individual's methylation capacity. Key components covered by a Methylation Test may include:
Examining the genetic code to analyze individual characteristics lifestyle, design balancing food and nutrition including the exercise that is most appropriate for you. It can also predict the risk of diseases that will be caused by genetic factors to be used as information to reduce the risk of disease in the future.
Confirm the paternity of your unborn baby with a 99.9% accurate test that requires only blood samples from the mother and alleged father
A Paternity DNA Test is used to determine who is the genetic Father of a Child or Children
Non-Invasive Prenatal Testing for detecting fetal chromosomal aneuploidies from maternal blood, such as Down syndrome, Edward syndrome, and Patau syndrome
Carrier screening for Monogenic disease
Thalassemia mutations detection for > 508
Thalassemia mutation including common
Alpha- and Beta-thalassemia
Newborn genetic screening for 112 genetic diseases.
Newborn 48 metabolic disorders screening
Clinical whole exome sequencing for detection and diagnosis of rare diseases
Detection of gene mutations that result in a higher-than-normal chance of developing cancer which can help predict the risk of cancer.
Do you experience symptoms of gut microbiome imbalance?
Signs may include:
Did you know that the gut houses over 5,000 types of microorganisms? Our Gut Microbiome Screening examines more than 100 different microorganisms in your body.
This screening uses stool samples to evaluate gut bacteria, providing key insights into:
Importance of Gut Microbiome Screening
A balanced gut microbiome supports a protective mucus layer that guards against harmful bacteria and inflammation. An imbalance may elevate the risk of diseases such as inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS), and increase susceptibility to conditions triggered by pathogenic bacteria.
How the Test is Conducted
The test involves Next Generation Sequencing (NGS) and uses a swab similar to an ATK test. It can be completed at home or in the hospital. If done at home, a hospital staff member will collect the swab and send it to Korea for analysis. The process is quick and straightforward.
Benefits of the Screening
Next Steps After Results
A doctor will interpret your results,
Explore Your Ancestry, Optimize Your Health, and Embrace Your Unique Genetic Traits with Our Comprehensive DNA Testing Service
mail@medex.co.th
Immediate medical care will be provided if your test results are positive. Enjoy stress-free doctor consultations at MedEx Neo Clinic with prices starting from just 750 THB.
You can also access a pool of over 3,000 top specialists at JCI (US)-accredited Thai hospitals in the MedEx Network via our tele-consultation services.
Additionally, we offer doorstep delivery of essential healthcare supplies.
Unveil Your DNA: Discover the Secrets Within
This is a medical test that couples or individuals planning to have a baby can undergo before conception. It is designed to identify potential genetic disorders in the baby's DNA. The primary goal is to provide reliable and early information about the fetal genetic health without resorting to invasive procedures that might carry the risk of miscarriage. This test helps parents make informed decisions about their pregnancy and prepares them for any potential health challenges their child may face.
SENTIS Hereditary Cancer Screening is a specialized DNA test that focuses on detecting genetic mutations associated with hereditary or familial cancers. This test helps individuals understand their genetic predisposition to certain types of cancer. By analyzing an individual's genetic blueprint, SENTIS aims to provide early insights into the risk of developing hereditary cancers. Armed with this knowledge, individuals can take proactive measures for cancer prevention and early detection, potentially saving lives.
Hereditary DNA testing is a comprehensive examination of an individual's genetic makeup. By analyzing an individual's DNA, this test offers insights into one's unique genetic blueprint. It can reveal information about ancestry, traits, and potential health risks, including genetic predispositions to various conditions. This test empowers individuals to gain a deeper understanding of themselves on a genetic level, which can be valuable for making informed decisions about their lifestyle, health, and wellness.
Genetic testing is a broad category of medical and scientific examinations that involve analyzing an individual's DNA. These tests can reveal information about an individual's genetic makeup, including their susceptibility to certain diseases, ancestry, and genetic traits. Genetic testing has applications in various fields, such as medicine, ancestry research, and personalized healthcare. It helps individuals and healthcare providers make informed decisions regarding health, family planning, and overall well-being.
Frequently Asked Questions
Genetic disorders arise due to alterations in an individual's genetic material, encompassing their genes and chromosomes. Aneuploidy characterizes a condition where there are either surplus or deficient chromosomes. Trisomy denotes the presence of an extra chromosome, while monosomy signifies the absence of one chromosome. Inherited disorders, conversely, result from genetic changes termed mutations. These disorders comprise conditions like sickle cell disease, cystic fibrosis, Tay-Sachs disease, and numerous others. Typically, for an offspring to be affected by an inherited disorder, both parents must carry the same mutated gene.
Prenatal genetic testing is a medical examination performed during pregnancy to assess the genetic health and development of the fetus. It aims to identify potential genetic abnormalities, chromosomal disorders, or inherited conditions in the unborn child. Prenatal genetic testing offers valuable information to expectant parents and healthcare providers, aiding in making informed decisions about the pregnancy, including choices about the continuation of the pregnancy, preparing for medical interventions, or planning for the care of a child with special needs.
1. Screening Tests: Prenatal screening tests are typically the first step in assessing the risk of a fetus having a genetic disorder. These tests are non-invasive and include options like non-invasive prenatal testing (NIPT), maternal serum screening (also known as triple or quad screen), and ultrasound examinations. They provide information about the likelihood of the fetus having certain genetic conditions. If a screening test suggests an increased risk, further diagnostic testing may be recommended.
2. Diagnostic Tests: Prenatal diagnostic tests are more invasive and definitive. They are performed when a screening test indicates a higher risk of a genetic disorder or when there are other indications for a diagnostic assessment. Common diagnostic tests include chorionic villus sampling (CVS) and amniocentesis. These tests directly examine the genetic material of the fetus, providing a definitive diagnosis of genetic conditions, chromosomal abnormalities, or other genetic disorders.
Embark on a unique journey of self-discovery with our DNA testing services. Uncover your ancestral origins, gain insights into your health, and explore the fascinating world of your genetic traits. Your DNA holds the key to your past, present, and future, and we're here to help you decode it.
Empower yourself with personalized genetic insights. Our DNA testing service offers a window into your genetic makeup, helping you make informed decisions about your health and lifestyle. It's time to take control of your destiny and embrace the power of your DNA.
Unveil the mysteries of your genetic code with our cutting-edge DNA testing. Gain valuable knowledge about your ancestry, health predispositions, and unique traits. Armed with this information, you can make proactive choices for a healthier and more fulfilling life.
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Last updated: June 30th, 2022
If you’re dissatisfied with a purchase, We invite You to read our refund and return policy. The following conditions apply to any items or services that you bought from Us.
The meanings of words with the first letter capitalized are defined as follows. The following definitions shall have the same meaning regardless of whether they appear in singular or plural.
For the purposes of this Refund and Return Policy:
You are entitled to cancel Your Order for Packages as per the following terms:
3.1 If you cancel an Order before 4 PM (GMT+7) the next day after making the payment, you can receive an 80% refund. For example, if you want to cancel your reservation, for example, after making it on March 25th, 2022 at 10 AM; You may do so and receive an 80% refund if you notify the company before 4:00 PM on March 26th, 2022.
3.2 If you cancel an Order before 4 PM (GMT+7) one day before the appointment date, you will receive a 50% refund. For example, if you scheduled a lab test for March 29th at 10 AM, you may cancel and receive a 50 percent refund if you notify the laboratory by 4 PM on March 28th, 2022.
3.3 The refund is not allowed if you cancel the order after 4 PM (GMT+7) one day before the appointment date.
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MedEx Ventures Co., Ltd, 10-95/97 Trendy Building, 6th Floor, Soi Sukhumvit 13 Sukhumvit Road, Khlong Toei Nuea, Watthana, Bangkok 10110
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