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SDHD Gene Paragangliomas Type 1 With or Without Deafness Genetic Test Cost

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

-21%

The “SDHD Gene Paragangliomas Type 1 With or Without Deafness Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the SDHD gene, which are linked to the development of paragangliomas type 1. Paragangliomas are rare, often hereditary tumors that can occur in various parts of the body, including the head and neck. Some individuals with mutations in the SDHD gene may also experience hearing loss, either as a part of the condition or independently. This genetic test is crucial for individuals with a family history of paragangliomas or early onset deafness, as it can provide vital information for managing their health. The test is priced at 4400 AED and is conducted with the highest standards of accuracy and confidentiality at DNA Labs UAE.

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  • This test is not intended for medical diagnosis or treatment
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SDHD Gene Paragangliomas Type 1 with or without Deafness Genetic Test

At DNA Labs UAE, we offer the SDHD Gene Paragangliomas Type 1 with or without Deafness Genetic Test. This test helps in detecting mutations or changes in the SDHD gene, which is associated with paragangliomas, rare tumors that develop in nerve tissue in areas like the head, neck, and abdomen. The SDHD gene is also linked to the development of deafness in some individuals with paragangliomas.

Test Components and Price

The SDHD Gene Paragangliomas Type 1 with or without Deafness Genetic Test costs 4400.0 AED. The test is performed using next-generation sequencing (NGS) technology.

Sample Condition and Report Delivery

The test requires a blood or extracted DNA sample. Alternatively, one drop of blood can be collected on an FTA card. The report is typically delivered within 3 to 4 weeks.

Test Type and Referring Doctor

The SDHD Gene Paragangliomas Type 1 with or without Deafness Genetic Test is a cancer genetic test. It is referred by oncologists.

Test Department

The test is conducted in our Genetics department.

Pre Test Information

Prior to the test, we recommend providing the clinical history of the patient who is undergoing the SDHD Gene Paragangliomas Type 1 with or without Deafness Genetic Test. Additionally, a genetic counseling session is conducted to create a pedigree chart of family members affected by SDHD Gene Paragangliomas Type 1 with or without Deafness NGS Genetic DNA Test gene SDHD.

Test Details

The SDHD Gene Paragangliomas Type 1 with or without Deafness Genetic Test utilizes next-generation sequencing (NGS) technology to analyze the DNA sequence of the SDHD gene. This helps in identifying any mutations or changes that may be present. The test is typically performed on a blood or saliva sample. The results aid in diagnosing individuals with paragangliomas and determining the risk of deafness associated with the SDHD gene mutation. This information is valuable in guiding medical management and treatment decisions for individuals and their families.

Test Name SDHD Gene Paragangliomas type 1 with or without deafness 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 Cancer
Doctor Oncologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SDHD Gene Paragangliomas type 1, with or without deafness NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SDHD Gene Paragangliomas type 1, with or without deafness NGS Genetic DNA Test gene SDHD
Test Details

SDHD gene paragangliomas type 1, with or without deafness NGS genetic test is a type of genetic test that is used to detect mutations or changes in the SDHD gene. This gene is associated with paragangliomas, which are rare tumors that develop in the nerve tissue of certain areas of the body, such as the head, neck, and abdomen.

The SDHD gene is also associated with the development of deafness in some individuals with paragangliomas. This genetic test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the SDHD gene and identify any mutations or changes that may be present.

The test is typically performed on a blood or saliva sample, and the results can help diagnose individuals with paragangliomas and determine the risk of deafness associated with the SDHD gene mutation. This information can be useful for guiding medical management and treatment decisions for individuals and their families.