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PRKCH Gene Cerebral Infarction Susceptibility to Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The PRKCH gene, associated with the protein kinase C eta type, has been linked to an increased susceptibility to cerebral infarction, a type of ischemic stroke where blood flow to a part of the brain is obstructed, leading to brain tissue damage. Given the significant role genetics play in the risk of developing cerebral infarction, genetic testing for variations in the PRKCH gene can provide crucial information for individuals concerned about their stroke risk.

DNA Labs UAE offers a specialized genetic test focused on the PRKCH gene to assess an individual’s susceptibility to cerebral infarction. This test is particularly beneficial for those with a family history of stroke or identified risk factors, enabling them to take preventive measures based on their genetic predisposition. The cost of the test is 4400 AED, which reflects the comprehensive analysis and personalized risk assessment provided.

By opting for this test, individuals can gain valuable insights into their genetic makeup, empowering them with the information needed to make informed health decisions. It’s a proactive approach to health management, allowing for personalized preventive strategies to reduce the risk of cerebral infarction.

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  • This test is not intended for medical diagnosis or treatment
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PRKCH Gene Cerebral Infarction Susceptibility to Genetic Test

Are you concerned about your risk of cerebral infarction? DNA Labs UAE offers the PRKCH Gene Cerebral Infarction Susceptibility Genetic Test to help you understand your genetic predisposition to this condition.

Test Details

The PRKCH gene encodes for a protein kinase C eta (PKC eta) enzyme, which plays a crucial role in various cellular processes, including cell growth, differentiation, and apoptosis. Mutations in the PRKCH gene have been linked to an increased risk of cerebral infarction, a type of stroke caused by blocked blood flow to the brain.

Our PRKCH Gene Cerebral Infarction Susceptibility Genetic Test utilizes next-generation sequencing (NGS) technology to analyze a large number of genes simultaneously. This advanced testing method allows us to identify mutations in the PRKCH gene that may increase your risk of cerebral infarction. Additionally, we can also detect mutations in other genes associated with an elevated risk of stroke or other cardiovascular diseases.

Test Components and Price

Test Name: PRKCH Gene Cerebral Infarction Susceptibility to Genetic Test

  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: 4400.0 AED

Sample Collection

You can provide a blood sample or extracted DNA for this genetic test. Alternatively, you can use one drop of blood on an FTA card.

Report Delivery

Once your sample is received, our laboratory will process the test and deliver the report within 3 to 4 weeks.

Pre-Test Information

Before undergoing the PRKCH Gene Cerebral Infarction Susceptibility Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by PRKCH Gene Cerebral Infarction Susceptibility.

Test Department and Doctor

Test Department: Genetics

Doctor: Neurologist

Diagnosis and Symptoms

Cerebral infarction, or ischemic stroke, occurs when blood flow to the brain is blocked, leading to brain cell damage. Symptoms may include sudden weakness or numbness in the face, arm, or leg, difficulty speaking or understanding speech, severe headache, dizziness, and loss of coordination.

Post-Test Recommendations

If a mutation is identified in the PRKCH gene through NGS genetic testing, individuals may be advised to take steps to reduce their risk of stroke. This may include maintaining a healthy lifestyle, managing blood pressure and cholesterol levels, and taking medication if necessary. Genetic counseling may also be recommended to help individuals understand the implications of their genetic test results and make informed decisions about their health.

Don’t wait to take control of your health. Contact DNA Labs UAE today to schedule your PRKCH Gene Cerebral Infarction Susceptibility Genetic Test.

Test Name PRKCH Gene Cerebral infarction susceptibility to Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PRKCH Gene Cerebral infarction, susceptibility to NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PRKCH Gene Cerebral infarction, susceptibility to
Test Details

The PRKCH gene is a gene that encodes for a protein kinase C eta (PKC eta) enzyme. This enzyme is involved in the regulation of various cellular processes, including cell growth, differentiation, and apoptosis. Mutations in the PRKCH gene have been associated with an increased risk of cerebral infarction, which is a type of stroke that occurs when blood flow to the brain is blocked.

NGS genetic testing is a type of genetic testing that uses next-generation sequencing technology to analyze a large number of genes simultaneously. This type of testing can be used to identify mutations in the PRKCH gene that may increase the risk of cerebral infarction. NGS genetic testing can also be used to identify mutations in other genes that may be associated with an increased risk of stroke or other cardiovascular diseases.

If a mutation is identified in the PRKCH gene through NGS genetic testing, individuals may be advised to take steps to reduce their risk of stroke, such as maintaining a healthy lifestyle, managing blood pressure and cholesterol levels, and taking medication if necessary. In some cases, genetic counseling may also be recommended to help individuals understand the implications of their genetic test results and make informed decisions about their health.