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JAM3 Gene Hemorrhagic Destruction of the Brain Subependymal Calcification and Cataracts Genetic Test

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

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The “JAM3 Gene Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts Genetic Test” is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the JAM3 gene. Mutations in this gene are associated with a rare genetic disorder characterized by severe neurological damage, including hemorrhagic destruction of brain tissue, subependymal calcification (a condition where calcium deposits form beneath the lining of the ventricles of the brain), and the early onset of cataracts. These symptoms result from the impaired function of the JAM3 protein, which plays a crucial role in maintaining the integrity of blood vessels and epithelial barriers in the brain.

This genetic test is pivotal for early diagnosis and management of the condition, offering families critical information for genetic counseling and potential treatment strategies. The test cost is 4400 AED and is conducted in the state-of-the-art facilities of DNA Labs UAE, which is equipped with the latest in genetic testing technology to ensure accurate and reliable results. Patients seeking this test may require a referral from a healthcare provider, and it is recommended to discuss the potential implications of the test results with a genetic counselor or a specialist in genetics.

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JAM3 Gene Hemorrhagic Destruction of the Brain Subependymal Calcification and Cataracts Genetic Test

Are you or your loved ones experiencing symptoms such as brain destruction, subependymal calcification, and cataracts? If so, the JAM3 Gene Hemorrhagic Destruction of the Brain Subependymal Calcification and Cataracts Genetic Test may provide valuable insights.

Test Details

The JAM3 gene is associated with a rare genetic disorder known as Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts (HDBSC). This disorder is characterized by the progressive destruction of brain tissue, the presence of calcium deposits in the lining of the brain’s ventricles (subependymal calcification), and the development of cataracts in the eyes.

NGS (Next-Generation Sequencing) genetic testing is a cutting-edge technique that allows for the analysis of multiple genes simultaneously. This enables the detection of genetic variations or mutations that may be responsible for a particular disorder. In the case of HDBSC, NGS genetic testing can identify mutations in the JAM3 gene, which is associated with this disorder.

By analyzing an individual’s DNA sample, NGS genetic testing can provide valuable information about the presence of mutations in the JAM3 gene. This information can help confirm a diagnosis of HDBSC, especially in cases where symptoms are atypical or other diagnostic methods have been inconclusive.

Test Components and Price

The JAM3 Gene Hemorrhagic Destruction of the Brain Subependymal Calcification and Cataracts Genetic Test is available for a cost of AED 4400.0. The test can be conducted using blood or extracted DNA, or even a single drop of blood on an FTA card.

Report Delivery and Method

After the test is conducted, the report will be delivered within 3 to 4 weeks. The test utilizes NGS technology, which ensures accurate and efficient analysis of the JAM3 gene.

Test Type and Doctor

The JAM3 Gene Hemorrhagic Destruction of the Brain Subependymal Calcification and Cataracts Genetic Test falls under the category of Vascular Diseases. It is recommended to consult a General Physician for this test.

Test Department and Pre-Test Information

The JAM3 Gene Hemorrhagic Destruction of the Brain Subependymal Calcification and Cataracts Genetic Test is conducted by the Genetics department. Before undergoing the test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to create a pedigree chart of family members affected by the disorder.

Importance of Genetic Testing

It is crucial to note that genetic testing should be performed by a qualified healthcare professional who can provide appropriate counseling and support before and after the test. The results of genetic testing can have significant implications for individuals and their families. Therefore, it is essential to have a clear understanding of the potential risks, benefits, and limitations of testing.

If you or your loved ones are experiencing symptoms related to Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts, consider the JAM3 Gene Hemorrhagic Destruction of the Brain Subependymal Calcification and Cataracts Genetic Test. It may provide the answers you need for a proper diagnosis and treatment plan.

Test Name JAM3 Gene Hemorrhagic destruction of the brain subependymal calcification and cataracts Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Vascular Diseases
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for JAM3 Gene Hemorrhagic destruction of the brain, subependymal calcification, and cataracts NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with JAM3 Gene Hemorrhagic destruction of the brain, subependymal calcification, and cataracts NGS Genetic DNA Test gene JAM3
Test Details

The JAM3 gene is associated with a rare genetic disorder called Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts (HDBSC). This disorder is characterized by the progressive destruction of brain tissue, the presence of calcium deposits in the lining of the brain’s ventricles (subependymal calcification), and the development of cataracts in the eyes.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, allowing for the detection of genetic variations or mutations that may be responsible for a particular disorder. In the case of HDBSC, NGS genetic testing can be used to identify mutations in the JAM3 gene, which is known to be associated with this disorder.

By analyzing an individual’s DNA sample, NGS genetic testing can provide information about the presence of mutations in the JAM3 gene, helping to confirm a diagnosis of HDBSC. This can be particularly useful in cases where the symptoms are atypical or when other diagnostic methods have been inconclusive.

It’s important to note that genetic testing should be performed by a qualified healthcare professional who can provide appropriate counseling and support both before and after the test. Genetic testing results can have significant implications for individuals and their families, so it’s crucial to have a clear understanding of the potential risks, benefits, and limitations of testing.