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IFT80 Gene Short-Rib Thoracic Dysplasia Type 2 with or Without Polydactyly Genetic Test Cost

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

-21%

The “IFT80 Gene Short-Rib Thoracic Dysplasia Type 2 with or Without Polydactyly Genetic Test” is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the IFT80 gene. These mutations are known to cause Short-Rib Thoracic Dysplasia Type 2 (SRTD2), a rare genetic disorder characterized by short ribs, shortening of long bones, narrow chest, and sometimes, extra fingers or toes (polydactyly). This test is crucial for early diagnosis, allowing for appropriate management and genetic counseling for affected families. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the presence of the specific gene mutation.

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IFT80 Gene Short-rib thoracic dysplasia type 2 with or without polydactyly Genetic Test

At DNA Labs UAE, we offer the IFT80 Gene Short-rib thoracic dysplasia type 2 with or without polydactyly Genetic Test. This test helps in diagnosing a rare genetic disorder known as short-rib thoracic dysplasia type 2 with or without polydactyly (SRTD2).

SRTD2 affects the development of various body systems, including the skeleton, lungs, and kidneys. To analyze this disorder, we use NGS (Next-Generation Sequencing) technology, which allows for a more comprehensive evaluation of genetic disorders by analyzing multiple genes simultaneously.

Test Details

The IFT80 gene is specifically associated with SRTD2. By performing an NGS genetic test on an individual suspected of having SRTD2, healthcare professionals can confirm the diagnosis, provide genetic counseling, and potentially guide treatment decisions.

Our test requires a sample of blood or extracted DNA, or one drop of blood on an FTA Card. The cost of the IFT80 Gene Short-rib thoracic dysplasia type 2 with or without polydactyly Genetic Test is AED 4400.0.

The test results are usually delivered within 3 to 4 weeks. Once the results are ready, they will be provided to you in a detailed report.

Pre Test Information

Prior to undergoing the IFT80 Gene Short-rib thoracic dysplasia type 2 with or without polydactyly Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by SRTD2. This information will help in understanding the inheritance pattern and risk assessment.

Consultation and Genetic Counseling

It is crucial to consult with a healthcare professional or a genetic counselor before undergoing any genetic testing procedure. They will be able to explain the benefits, limitations, and implications of the test. Genetic counseling can provide valuable information about the condition, its inheritance, and the potential impact on the patient and their family members.

By testing family members, it is possible to determine their risk of passing on the condition to future generations. This information can be crucial for family planning and making informed decisions.

At DNA Labs UAE, we prioritize providing accurate and reliable genetic testing services. Our team of experts, including pediatricians and geneticists, ensures that you receive the best possible care and guidance throughout the testing process.

For more information about the IFT80 Gene Short-rib thoracic dysplasia type 2 with or without polydactyly Genetic Test or to schedule an appointment, please contact DNA Labs UAE.

Test Name IFT80 Gene Short-rib thoracic dysplasia type 2 with or without polydactyly 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for IFT80 Gene Short-rib thoracic dysplasia type 2 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IFT80 Gene Short-rib thoracic dysplasia type 2 with or without polydactyly NGS Genetic DNA Test gene IFT80
Test Details

The IFT80 gene is associated with a rare genetic disorder called short-rib thoracic dysplasia type 2 with or without polydactyly (SRTD2). This disorder affects the development of various body systems, including the skeleton, lungs, and kidneys.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of genetic disorders. In the case of SRTD2, NGS testing can identify mutations or variations in the IFT80 gene that may be causing the disorder.

By performing an NGS genetic test on an individual suspected of having SRTD2, healthcare professionals can confirm the diagnosis, provide genetic counseling, and potentially guide treatment decisions. Additionally, testing family members can help determine their risk of passing on the condition to future generations.

It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and implications of genetic testing before undergoing any testing procedure.

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