P3H1 Gene Osteogenesis imperfecta type 8 Genetic Test
At DNA Labs UAE, we offer the P3H1 Gene Osteogenesis imperfecta type 8 Genetic Test for individuals who suspect they may have this rare form of Osteogenesis imperfecta (OI). This genetic test analyzes the P3H1 gene, which is responsible for producing an enzyme called prolyl 3-hydroxylase 1 that plays a crucial role in collagen synthesis.
Osteogenesis imperfecta type 8 is caused by mutations in the P3H1 gene. To diagnose this condition, we use NGS (Next-Generation Sequencing) technology, which allows us to analyze multiple genes simultaneously. By identifying mutations in the P3H1 gene through NGS genetic testing, our healthcare professionals can provide a more accurate diagnosis of OI type 8.
The cost of the P3H1 Gene Osteogenesis imperfecta type 8 Genetic Test is 4400.0 AED. The test can be performed on either blood or extracted DNA, or even just one drop of blood on an FTA card. The report delivery time is typically 3 to 4 weeks.
Before undergoing the P3H1 Gene Osteogenesis imperfecta type 8 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with the P3H1 Gene Osteogenesis imperfecta type 8 NGS Genetic DNA Test gene P3H1.
By utilizing NGS genetic testing, we can provide a more comprehensive analysis of the genetic makeup, enabling the identification of specific mutations that may be causing the disease. This information is not only valuable for an accurate diagnosis but also for genetic counseling, predicting disease severity, and potentially guiding treatment options.
If you suspect you or a family member may have Osteogenesis imperfecta type 8, we recommend reaching out to a dermatologist who can refer you to our Genetics Test Department for further evaluation. Our team of professionals is dedicated to providing accurate and timely genetic testing services.
| Test Name | P3H1 Gene Osteogenesis imperfecta type 8 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 P3H1 Gene Osteogenesis imperfecta type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with P3H1 Gene Osteogenesis imperfecta type 8 NGS Genetic DNA Test gene P3H1 |
| Test Details | The P3H1 gene is responsible for producing an enzyme called prolyl 3-hydroxylase 1, which plays a crucial role in collagen synthesis. Osteogenesis imperfecta (OI) type 8 is a rare form of OI that is caused by mutations in the P3H1 gene. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of OI type 8, NGS genetic testing can be used to identify mutations in the P3H1 gene. This testing method allows for a more comprehensive analysis of the genetic makeup, enabling the identification of specific mutations that may be causing the disease. By identifying mutations in the P3H1 gene through NGS genetic testing, healthcare professionals can provide a more accurate diagnosis of OI type 8. This information can also be used for genetic counseling, predicting disease severity, and potentially guiding treatment options. |
