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IFITM5 Gene Osteogenesis Imperfecta Type 5 Genetic Test Cost

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

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The IFITM5 gene plays a crucial role in bone development and mineralization, and mutations in this gene are associated with Osteogenesis Imperfecta (OI) Type 5. Osteogenesis Imperfecta, also known as brittle bone disease, is a group of genetic disorders characterized by fragile bones that break easily. Type 5 is distinguished from other types by certain unique clinical features, including hyperplastic callus formation, calcification of the interosseous membrane of the forearm, and an abnormality of the toes.

DNA Labs UAE offers a genetic test specifically designed to identify mutations in the IFITM5 gene, providing a definitive diagnosis of Osteogenesis Imperfecta Type 5. This test is crucial for affected individuals and their families for several reasons. Firstly, it allows for a precise diagnosis, distinguishing OI Type 5 from other types of OI and other bone disorders. Secondly, it provides valuable information for genetic counseling, helping families understand the risk of OI Type 5 in future pregnancies. Lastly, the test results can inform treatment decisions and management plans to improve the quality of life for those affected.

The cost of the IFITM5 gene Osteogenesis Imperfecta Type 5 genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the specific mutations in the IFITM5 gene associated with the condition. Given the complexity and the specialized nature of this genetic testing, the price reflects the advanced technology and expertise involved in providing accurate and reliable results.

Individuals considering this test are encouraged to discuss it with their healthcare provider to understand its benefits and implications fully.

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IFITM5 Gene Osteogenesis imperfecta type 5 Genetic Test

Are you or someone you know experiencing symptoms of Osteogenesis Imperfecta type 5 (OI type 5)? DNA Labs UAE offers the IFITM5 Gene Osteogenesis imperfecta type 5 Genetic Test to help diagnose this rare genetic disorder.

Test Details

The IFITM5 gene is associated with Osteogenesis Imperfecta type 5, a condition characterized by brittle bones and skeletal abnormalities. Our NGS (Next Generation Sequencing) genetic testing method allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of OI type 5, this test can identify mutations or variations in the IFITM5 gene that may be responsible for the condition.

Components

  • Test Name: IFITM5 Gene Osteogenesis imperfecta type 5 Genetic Test
  • 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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information

Prior to the IFITM5 Gene Osteogenesis imperfecta type 5 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the IFITM5 Gene Osteogenesis imperfecta type 5 NGS Genetic DNA Test gene IFITM5.

Why Choose NGS Genetic Testing?

NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in specific genes. This can help confirm a diagnosis, provide information about disease severity, and guide treatment decisions. If you suspect that you or someone you know may have OI type 5, a healthcare professional or genetic counselor can help determine if NGS genetic testing is appropriate and guide you through the testing process.

It is important to note that genetic testing should always be done under the guidance of a healthcare professional to ensure accurate interpretation of results and appropriate counseling.

Test Name IFITM5 Gene Osteogenesis imperfecta type 5 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for IFITM5 Gene Osteogenesis imperfecta type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IFITM5 Gene Osteogenesis imperfecta type 5 NGS Genetic DNA Test gene IFITM5
Test Details

The IFITM5 gene is associated with Osteogenesis Imperfecta type 5 (OI type 5), which is a rare genetic disorder characterized by brittle bones and skeletal abnormalities.

NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of OI type 5, NGS genetic testing can be used to identify mutations or variations in the IFITM5 gene that may be responsible for the condition.

NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in specific genes. This can help in confirming a diagnosis, providing information about disease severity, and guiding treatment decisions.

If you suspect that you or someone you know may have OI type 5, a healthcare professional or genetic counselor can help determine if NGS genetic testing is appropriate and guide you through the testing process. It is important to note that genetic testing should always be done under the guidance of a healthcare professional to ensure accurate interpretation of results and appropriate counseling.

SKU: TEST-3183 Category:

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