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P3H1 Gene Osteogenesis Imperfecta Type 8 Genetic Test Cost

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

-21%

The P3H1 gene osteogenesis imperfecta type 8 genetic test is a specialized diagnostic tool designed to identify mutations in the P3H1 gene, which are linked to osteogenesis imperfecta type 8 (OI type 8). Osteogenesis imperfecta, also known as brittle bone disease, is a group of genetic disorders that primarily affect the bones, leading to their increased fragility and susceptibility to fractures. Type 8 is a severe form of the condition, characterized by bone deformities, reduced bone mass, and other connective tissue symptoms.

This genetic test is crucial for the accurate diagnosis of OI type 8, enabling healthcare providers to tailor treatment plans and management strategies specific to the needs of the patient. Early diagnosis through genetic testing can significantly improve the quality of life for individuals with OI type 8 by implementing preventive measures against fractures, providing physical therapy, and other supportive care as needed.

The test is available at DNA Labs UAE, a leading facility in genetic diagnostics and research. The cost of the P3H1 gene osteogenesis imperfecta type 8 genetic test is 4400 AED. DNA Labs UAE employs state-of-the-art technology and follows stringent protocols to ensure the accuracy and reliability of the test results, providing patients and their families with crucial information for managing the condition.

Description

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.