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FKBP10 Gene Osteogenesis Imperfecta Type 11 Genetic Test Cost

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

-21%

The FKBP10 gene plays a crucial role in the development and maintenance of the body’s connective tissues, including bones. Mutations in the FKBP10 gene can lead to Osteogenesis Imperfecta Type 11 (OI Type 11), a rare but severe form of brittle bone disease. This condition is characterized by fragile bones that break easily, often with little or no apparent cause, along with other possible symptoms such as joint laxity, muscle weakness, and hearing loss.

To diagnose this specific type of Osteogenesis Imperfecta, a genetic test is available that screens for mutations in the FKBP10 gene. This test is crucial for confirming the diagnosis of OI Type 11, understanding the risk of passing the condition to future generations, and guiding treatment decisions.

In the UAE, this specialized genetic test is offered by DNA Labs UAE, a leading provider of genetic testing services. The cost of the FKBP10 Gene Osteogenesis Imperfecta Type 11 Genetic Test is 4400 AED. This comprehensive test is conducted with a high level of accuracy and confidentiality, ensuring that individuals and families affected by or at risk of OI Type 11 receive the vital information they need for managing the condition.

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FKBP10 Gene Osteogenesis imperfecta type 11 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 FKBP10 Gene Osteogenesis imperfecta type 11 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FKBP10 Gene Osteogenesis imperfecta type 11 NGS Genetic DNA Test gene FKBP10.

Test Details

The FKBP10 gene is associated with Osteogenesis Imperfecta Type 11 (OI type 11), which is a rare genetic disorder characterized by brittle bones, short stature, and other skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be responsible for a particular condition.

In the case of OI type 11, NGS genetic testing can be used to identify mutations or variations in the FKBP10 gene that may be causing the disorder. NGS genetic testing involves sequencing the DNA of an individual, usually through a blood or saliva sample, and analyzing it for specific variations in the FKBP10 gene. This can help in confirming a diagnosis of OI type 11 and can also provide information about the specific mutation present in the gene.

Genetic testing for OI type 11 can be useful for individuals who have symptoms consistent with the disorder, as well as for their family members who may be at risk of carrying the same genetic mutation. It can help in providing a definitive diagnosis, guiding treatment decisions, and offering genetic counseling to affected individuals and their families.

Test Name FKBP10 Gene Osteogenesis imperfecta type 11 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 FKBP10 Gene Osteogenesis imperfecta type 11 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FKBP10 Gene Osteogenesis imperfecta type 11 NGS Genetic DNA Test gene FKBP10
Test Details

The FKBP10 gene is associated with Osteogenesis Imperfecta Type 11 (OI type 11), which is a rare genetic disorder characterized by brittle bones, short stature, and other skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be responsible for a particular condition. In the case of OI type 11, NGS genetic testing can be used to identify mutations or variations in the FKBP10 gene that may be causing the disorder.

NGS genetic testing involves sequencing the DNA of an individual, usually through a blood or saliva sample, and analyzing it for specific variations in the FKBP10 gene. This can help in confirming a diagnosis of OI type 11 and can also provide information about the specific mutation present in the gene.

Genetic testing for OI type 11 can be useful for individuals who have symptoms consistent with the disorder, as well as for their family members who may be at risk of carrying the same genetic mutation. It can help in providing a definitive diagnosis, guiding treatment decisions, and offering genetic counseling to affected individuals and their families.

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