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PPIB Gene Osteogenesis Imperfecta Type 9 Genetic Test Cost

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

-21%

The PPIB Gene Osteogenesis Imperfecta Type 9 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at detecting mutations in the PPIB gene, which are associated with Osteogenesis Imperfecta (OI) Type 9. Osteogenesis Imperfecta, also known as brittle bone disease, is a group of genetic disorders characterized by bones that break easily, often with little or no apparent cause. Type 9 OI is a rare form of this condition and is distinguished by specific genetic mutations in the PPIB gene, which is essential for the proper formation and maintenance of collagen in the bone structure.

The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing the genetic material for the presence of mutations in the PPIB gene. A positive result indicates a mutation in the PPIB gene, confirming a diagnosis of Osteogenesis Imperfecta Type 9. This information is crucial for the management and treatment of the condition, allowing for personalized care plans that can significantly improve the quality of life for affected individuals.

The cost of the PPIB Gene Osteogenesis Imperfecta Type 9 Genetic Test at DNA Labs UAE is 4400 AED. This cost covers the entire testing process, from sample collection to genetic analysis and reporting. The investment in this test can provide families with essential information regarding the genetic basis of OI Type 9, enabling informed decisions about care and treatment options. Given the complexity and rarity of Osteogenesis Imperfecta Type 9, accessing accurate and timely genetic testing like the one offered by DNA Labs UAE is a critical step in the journey towards understanding and managing this condition.

Description

PPIB Gene Osteogenesis imperfecta type 9 Genetic Test

Components: PPIB Gene Osteogenesis imperfecta type 9 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: Clinical History of Patient who is going for PPIB Gene Osteogenesis imperfecta type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PPIB Gene Osteogenesis imperfecta type 9 NGS Genetic DNA Test gene PPIB

Test Details:

The PPIB gene is associated with a genetic disorder called osteogenesis imperfecta type 9 (OI9). Osteogenesis imperfecta (OI) is a group of genetic disorders characterized by fragile bones that break easily. OI9 is a rare form of OI caused by mutations in the PPIB gene. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific disorder. In the case of OI9, NGS genetic testing can be used to identify mutations in the PPIB gene that are responsible for causing the condition. By performing NGS genetic testing for OI9, healthcare professionals can provide an accurate diagnosis, determine the specific genetic mutation causing the disorder, and provide appropriate medical management and genetic counseling for affected individuals and their families.

Test Name	PPIB Gene Osteogenesis imperfecta type 9 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 PPIB Gene Osteogenesis imperfecta type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PPIB Gene Osteogenesis imperfecta type 9 NGS Genetic DNA Test gene PPIB
Test Details	The PPIB gene is associated with a genetic disorder called osteogenesis imperfecta type 9 (OI9). Osteogenesis imperfecta (OI) is a group of genetic disorders characterized by fragile bones that break easily. OI9 is a rare form of OI caused by mutations in the PPIB gene. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific disorder. In the case of OI9, NGS genetic testing can be used to identify mutations in the PPIB gene that are responsible for causing the condition. By performing NGS genetic testing for OI9, healthcare professionals can provide an accurate diagnosis, determine the specific genetic mutation causing the disorder, and provide appropriate medical management and genetic counseling for affected individuals and their families.