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CRTAP Gene Osteogenesis Imperfecta Type 7 Genetic Test Cost

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

-21%

The CRTAP Gene Osteogenesis Imperfecta Type 7 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the CRTAP gene, which are associated with Osteogenesis Imperfecta (OI) Type 7. Osteogenesis Imperfecta, also known as brittle bone disease, is a group of genetic disorders that mainly affect the bones, leading to frequent fractures, reduced bone density, and, in some cases, other health issues. Type 7 is a rare form of OI and involves mutations in the CRTAP gene, which plays a crucial role in collagen formation and bone strength.

This genetic test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to identify any abnormalities in the CRTAP gene. The results of this test can provide essential information for the diagnosis, management, and treatment planning of Osteogenesis Imperfecta Type 7. It can also be valuable for family planning and genetic counseling for families affected by this condition.

The cost of the CRTAP Gene Osteogenesis Imperfecta Type 7 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the CRTAP gene and provide reliable results. Individuals considering this test should consult with their healthcare provider to discuss its benefits and implications fully.

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CRTAP Gene Osteogenesis Imperfecta Type 7 Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing laboratory. Today, we will be discussing the CRTAP Gene Osteogenesis Imperfecta Type 7 Genetic Test. This test is specifically designed to diagnose Osteogenesis Imperfecta Type 7 (OI Type 7) and provide valuable insights into the condition. Let’s dive into the details:

Test Details

The CRTAP gene is associated with Osteogenesis Imperfecta Type 7 (OI Type 7), also known as OI with craniosynostosis. OI is a group of genetic disorders that affect the bones, making them brittle and prone to fractures. OI Type 7 is a rare form of OI characterized by craniosynostosis, which is the premature fusion of the skull bones.

Our state-of-the-art Next-Generation Sequencing (NGS) technology allows us to analyze multiple genes simultaneously, including the CRTAP gene. By conducting this comprehensive genetic test, we can confirm a diagnosis and identify any disease-causing mutations that may be present.

Test Components and Price

Our CRTAP Gene Osteogenesis Imperfecta Type 7 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

After conducting the test, we will deliver the comprehensive report within 3 to 4 weeks. Our NGS technology ensures accurate and reliable results.

Test Type and Doctor

The CRTAP Gene Osteogenesis Imperfecta Type 7 Genetic Test falls under the categories of Osteology, Dermatology, and Immunology Disorders. Our experienced dermatologists will oversee the test and provide expert guidance.

Test Department and Pre-Test Information

This genetic test is conducted in our Genetics department. Before the test, it is important to provide the clinical history of the patient who is undergoing the CRTAP Gene Osteogenesis Imperfecta Type 7 NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the CRTAP Gene Osteogenesis Imperfecta Type 7 NGS Genetic DNA Test gene CRTAP.

Who Can Benefit from the Test?

Genetic testing for OI Type 7 can be beneficial for individuals experiencing symptoms related to the condition. It can also be helpful for family members who may be at risk of carrying the disease-causing mutation. Furthermore, prenatal testing can be conducted in families with a known mutation to determine if the fetus is affected.

It is important to consult with a genetic counselor or healthcare provider to discuss the appropriateness and availability of NGS genetic testing for OI Type 7. They can provide more information about the specific test, its accuracy, limitations, and potential implications for individuals and their families.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule your CRTAP Gene Osteogenesis Imperfecta Type 7 Genetic Test and gain valuable insights into your genetic makeup.

Test Name CRTAP Gene Osteogenesis imperfecta type 7 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 CRTAP Gene Osteogenesis imperfecta type 7 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CRTAP Gene Osteogenesis imperfecta type 7 NGS Genetic DNA Test gene CRTAP
Test Details

The CRTAP gene is associated with Osteogenesis imperfecta type 7 (OI type 7), also known as OI with craniosynostosis. OI is a group of genetic disorders that affect the bones, causing them to be brittle and prone to fractures. OI type 7 is a rare form of OI that is characterized by craniosynostosis, which is the premature fusion of the skull bones.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of OI type 7, NGS can be used to analyze the CRTAP gene for any potential disease-causing mutations. This type of genetic testing can provide a comprehensive analysis of the gene, helping to confirm a diagnosis and identify any specific mutations that may be present.

Genetic testing for OI type 7 can be helpful for individuals who have symptoms suggestive of the condition, as well as for family members who may be at risk of carrying the disease-causing mutation. It can also be used for prenatal testing in families with a known mutation to determine if the fetus is affected.

It is important to consult with a genetic counselor or healthcare provider to discuss the appropriateness and availability of NGS genetic testing for OI type 7. They can provide more information about the specific test, its accuracy, limitations, and potential implications for individuals and their families.