ตรวจพันธุกรรมประเมินความเสี่ยงการเกิดโรคทางสมอง NEURO Genome

The genome, or genetic information (DNA), is the substance that stores genetic data, serving as a blueprint for living organisms passed down through generations. It determines the characteristics of our organs, shapes, appearances, and everything about us.
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Therefore, when many people are told they look like their father or mother, it is not a coincidence. It is the direct inheritance of genetics from both parents, resulting in eye color, skin color, height, and other traits, including the risk of various inherited diseases from our ancestors. When we have children, they will inherit half of our genetics and half from their other parent, continuing this way through every generation.
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Since genetics is immutable, knowing our genetic information allows us to adjust our lifestyle and environment to reduce the risk of diseases. The factors contributing to disease can be broadly categorized into three main parts: genetics (DNA), lifestyle, and environment.
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Currently, NEURO Genome testing can assess the risk of stroke, Alzheimer’s disease, Parkinson’s disease, migraine, and depression.
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If someone in your family has a neurological or brain disorder, it is advisable to undergo NEURO Genome testing. Some neurological and brain disorders can be genetically transmitted, meaning that genes causing these diseases can be passed from parents to children. Therefore, if you have family members with neurological conditions, genetic screening with NEURO Genome is significant and beneficial. Screening can lead to quicker diagnoses, targeted treatment planning, and better mental preparedness, aiding in decision-making regarding having children.
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<h2>Who Should Undergo Genetic Testing and NEURO Genome Testing?</h2>
Genetic testing is a way to understand our health baseline, so it can be done by anyone, especially those at risk, such as individuals with a direct family member suffering from a related illness or any chronic conditions. Testing can be performed from birth since each person’s genetics do not change throughout their lifetime; one test is sufficient as it remains constant into adulthood.
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Genetic testing informs us about our risk of developing certain diseases but does not indicate whether we currently have those diseases. Genetic testing can enhance the effectiveness of annual health check-ups. Knowing our disease risks allows us to select relevant health screenings. For example, if we are at risk for diabetes, we should focus on blood sugar testing and dietary lifestyle changes. Alternatively, if we have a condition, discovering that we are at high risk can provide supporting information for strict disease management to prevent exacerbation or recurrence.
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<h2>The Process of NEURO Genome Testing and Waiting for Results</h2>
The testing involves drawing approximately 6 milliliters of blood, with no need to fast or abstain from food. The samples are sent to a laboratory, and results typically take about 4-6 weeks.
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<h2>What Does It Mean If NEURO Genome Results Indicate a Risk of Disease?</h2>
NEURO Genome testing serves only to predict and assess disease risk; it is not a diagnostic test. If NEURO Genome results indicate genetic risk, improving lifestyle and environmental factors tailored to the individual can help reduce overall disease risk.
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Conversely, neglecting health or living in a highly polluted environment can also increase disease risk, even if genetic testing shows no genetic risk.
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Thus, understanding disease risk through NEURO Genome testing aids in more targeted disease prevention planning and health management. It is essential to have results interpreted by a qualified physician.

The genome, or genetic information (DNA), is the substance that stores genetic data, serving as a blueprint for living organisms passed down through generations. It determines the characteristics of our organs, shapes, appearances, and everything about us.

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Genetic Testing to Assess the Risk of Brain Diseases: NEURO Genome

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