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CA12 Gene Hyperchlorhidrosis Isolated Genetic Test Cost

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

-21%

The “CA12 Gene Hyperchlorhidrosis Isolated Genetic Test” is a specialized genetic analysis designed to detect mutations in the CA12 gene, which are associated with hyperchlorhidrosis. Hyperchlorhidrosis is a condition characterized by excessive sweating beyond what is typically required for body temperature regulation. This test is particularly valuable for individuals experiencing severe sweating without clear environmental or physiological causes, as it can confirm a genetic predisposition to this condition.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab. The sample is then analyzed to identify any genetic variations in the CA12 gene that may contribute to hyperchlorhidrosis.

The cost of the CA12 Gene Hyperchlorhidrosis Isolated Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test and the sophisticated technology and expertise required to accurately identify mutations in the CA12 gene. Patients considering this test should consult with a healthcare provider or a genetic counselor to discuss its implications, potential results, and the course of action based on the test outcomes.

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CA12 Gene Hyperchlorhidrosis isolated Genetic Test

At DNA Labs UAE, we offer the CA12 Gene Hyperchlorhidrosis isolated Genetic Test. This test aims to diagnose and provide valuable information for the treatment and management of hyperhidrosis, a medical condition characterized by excessive sweating.

Test Details

The CA12 Gene Hyperchlorhidrosis isolated Genetic Test focuses on analyzing and sequencing the DNA of an individual using next-generation sequencing (NGS) technology. This test specifically targets the CA12 gene, which is known to cause hyperhidrosis when mutated.

Test Components and Price

The cost of the CA12 Gene Hyperchlorhidrosis isolated Genetic Test is AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The report for the CA12 Gene Hyperchlorhidrosis isolated Genetic Test is typically delivered within 3 to 4 weeks.

Test Type and Department

The CA12 Gene Hyperchlorhidrosis isolated Genetic Test falls under the category of Metabolic Disorders. It is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is undergoing the CA12 Gene Hyperchlorhidrosis isolated Genetic Test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by Hyperchlorhidrosis, isolated.

When to Consider Genetic Testing

Genetic testing for hyperhidrosis is not typically performed as a first-line diagnostic tool. It is usually recommended when there is a strong suspicion of a genetic cause or when other diagnostic methods have been inconclusive. If you suspect you have CA12 gene hyperhidrosis, it is advised to consult with a genetic counselor or a healthcare professional specializing in genetics to discuss the appropriateness and availability of genetic testing in your specific case. They can guide you through the testing process and help interpret the results.

For more information or to schedule a CA12 Gene Hyperchlorhidrosis isolated Genetic Test, please contact DNA Labs UAE.

Test Name CA12 Gene Hyperchlorhidrosis isolated 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CA12 Gene Hyperchlorhidrosis, isolated NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperchlorhidrosis, isolated
Test Details

Hyperhidrosis is a medical condition characterized by excessive sweating. CA12 gene hyperhidrosis refers to a specific type of hyperhidrosis that is caused by mutations in the CA12 gene.

Isolated NGS genetic testing refers to the use of next-generation sequencing (NGS) technology to analyze and sequence the DNA of an individual. This type of genetic testing focuses specifically on a single gene or a small set of genes.

In the case of CA12 gene hyperhidrosis, isolated NGS genetic testing would involve sequencing the CA12 gene to identify any mutations or genetic variations that may be causing the hyperhidrosis. This type of testing can help diagnose the condition and provide valuable information for treatment and management options.

It’s important to note that genetic testing for hyperhidrosis is not typically performed as a first-line diagnostic tool. It is usually reserved for cases where there is a strong suspicion of a genetic cause or when other diagnostic methods have been inconclusive.

If you suspect you have CA12 gene hyperhidrosis, it is recommended to consult with a genetic counselor or a healthcare professional with expertise in genetics to discuss the appropriateness and availability of genetic testing in your specific case. They can guide you through the testing process and help interpret the results.