SP7 Gene Osteogenesis Imperfecta Type 12 Genetic Test sale cost 4400 AED
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SP7 Gene Osteogenesis Imperfecta Type 12 Genetic Test Cost

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

-21%

The SP7 Gene Osteogenesis Imperfecta Type 12 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SP7 gene, which are associated with Osteogenesis Imperfecta Type 12 (OI Type 12). 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 12 is a rare form of this condition, characterized by specific genetic anomalies in the SP7 gene that impact bone formation and health.

This test is crucial for individuals suspected of having OI Type 12, as it provides definitive genetic evidence of the condition, enabling accurate diagnosis and the possibility of tailored treatment plans. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect mutations in the SP7 gene.

At DNA Labs UAE, the cost of the SP7 Gene Osteogenesis Imperfecta Type 12 Genetic Test is set at 4400 AED. The price reflects the comprehensive nature of the test, including the sophisticated techniques used to identify the genetic markers associated with the condition. Given the complexity of Osteogenesis Imperfecta and the significant impact it has on individuals and families, this test represents a critical step towards managing the disease through personalized medicine approaches.

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SP7 Gene Osteogenesis imperfecta type 12 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 SP7 Gene Osteogenesis imperfecta type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SP7 Gene Osteogenesis imperfecta type 12 NGS Genetic DNA Test gene SP7

Test Details

The SP7 gene is associated with osteogenesis imperfecta type 12 (OI type 12), which is a rare genetic disorder characterized by brittle bones and other skeletal abnormalities. OI type 12 is caused by mutations in the SP7 gene, which encodes a transcription factor involved in the development and maintenance of bone tissue.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the context of OI type 12, an NGS genetic test can be performed to identify mutations in the SP7 gene, which can help in confirming a diagnosis of OI type 12.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This allows for the detection of specific genetic variations or mutations that may be responsible for a particular genetic disorder, such as OI type 12.

The results of an NGS genetic test for OI type 12 can provide valuable information for diagnosis, prognosis, and genetic counseling. It can help determine the specific genetic mutation responsible for the condition and can also help identify carriers of the mutation within a family.

It is important to note that NGS genetic testing for OI type 12 may not be widely available and may require consultation with a geneticist or genetic counselor. They can provide more information about the test, its availability, and the implications of the results.

Test Name SP7 Gene Osteogenesis imperfecta type 12 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 SP7 Gene Osteogenesis imperfecta type 12 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SP7 Gene Osteogenesis imperfecta type 12 NGS Genetic DNA Test gene SP7
Test Details

The SP7 gene is associated with osteogenesis imperfecta type 12 (OI type 12), which is a rare genetic disorder characterized by brittle bones and other skeletal abnormalities. OI type 12 is caused by mutations in the SP7 gene, which encodes a transcription factor involved in the development and maintenance of bone tissue.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the context of OI type 12, an NGS genetic test can be performed to identify mutations in the SP7 gene, which can help in confirming a diagnosis of OI type 12.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This allows for the detection of specific genetic variations or mutations that may be responsible for a particular genetic disorder, such as OI type 12.

The results of an NGS genetic test for OI type 12 can provide valuable information for diagnosis, prognosis, and genetic counseling. It can help determine the specific genetic mutation responsible for the condition and can also help identify carriers of the mutation within a family.

It is important to note that NGS genetic testing for OI type 12 may not be widely available and may require consultation with a geneticist or genetic counselor. They can provide more information about the test, its availability, and the implications of the results.

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