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WNT1 Gene Osteogenesis Imperfecta Type 15 Genetic Test Cost

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

-21%

The WNT1 gene plays a critical role in bone formation and development, and mutations in this gene can lead to Osteogenesis Imperfecta (OI) Type 15, a rare and severe form of the disorder characterized by bone fragility, skeletal abnormalities, and, in some cases, problems with the nervous system. To diagnose this condition accurately, genetic testing for mutations in the WNT1 gene is crucial.

At DNA Labs UAE, a specialized test is available for individuals suspected of having Osteogenesis Imperfecta Type 15. This test involves analyzing the WNT1 gene for specific mutations that are known to cause the condition. The procedure is designed to be thorough and is carried out in a state-of-the-art laboratory by professionals experienced in genetic diagnostics.

The cost of the WNT1 gene Osteogenesis Imperfecta Type 15 genetic test at DNA Labs UAE is 4400 AED. While the price might seem high, it’s important to consider the complexity of the testing process and the significant impact that a precise diagnosis can have on treatment planning and management of the condition. Early and accurate diagnosis can greatly assist in adopting the best care and interventions to manage symptoms and improve the quality of life for individuals with Osteogenesis Imperfecta Type 15.

Description

WNT1 Gene Osteogenesis Imperfecta Type 15 Genetic Test

Test Name: WNT1 Gene Osteogenesis Imperfecta Type 15 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 WNT1 Gene Osteogenesis Imperfecta Type 15 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNT1 Gene Osteogenesis Imperfecta Type 15 NGS Genetic DNA Test gene WNT1

Test Details: The WNT1 gene is associated with osteogenesis imperfecta type 15 (OI type 15), which is a rare genetic disorder characterized by brittle bones and skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the WNT1 gene and identify any mutations or variations that may be present. NGS testing is a high-throughput method that allows for the simultaneous analysis of multiple genes, including the WNT1 gene, in a single test. This type of testing can provide comprehensive genetic information and is particularly useful for identifying rare genetic disorders like OI type 15. By analyzing the WNT1 gene, NGS testing can detect various types of mutations, such as point mutations, insertions, deletions, and rearrangements. These mutations can disrupt the normal function of the WNT1 gene, leading to the development of OI type 15. NGS genetic testing for OI type 15 can be performed using a blood or saliva sample. The sample is sent to a laboratory where the DNA is extracted and sequenced using NGS technology. The resulting DNA sequence data is then analyzed for mutations or variations in the WNT1 gene. The identification of a mutation in the WNT1 gene through NGS testing can confirm a diagnosis of OI type 15. It can also help in genetic counseling and family planning by providing information about the inheritance pattern and the risk of passing the condition on to future generations. Additionally, NGS testing can aid in the development of personalized treatment plans and potential targeted therapies for individuals with OI type 15.

Test Name	WNT1 Gene Osteogenesis imperfecta type 15 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 WNT1 Gene Osteogenesis imperfecta type 15 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNT1 Gene Osteogenesis imperfecta type 15 NGS Genetic DNA Test gene WNT1
Test Details	The WNT1 gene is associated with osteogenesis imperfecta type 15 (OI type 15), which is a rare genetic disorder characterized by brittle bones and skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the WNT1 gene and identify any mutations or variations that may be present. NGS testing is a high-throughput method that allows for the simultaneous analysis of multiple genes, including the WNT1 gene, in a single test. This type of testing can provide comprehensive genetic information and is particularly useful for identifying rare genetic disorders like OI type 15. By analyzing the WNT1 gene, NGS testing can detect various types of mutations, such as point mutations, insertions, deletions, and rearrangements. These mutations can disrupt the normal function of the WNT1 gene, leading to the development of OI type 15. NGS genetic testing for OI type 15 can be performed using a blood or saliva sample. The sample is sent to a laboratory where the DNA is extracted and sequenced using NGS technology. The resulting DNA sequence data is then analyzed for mutations or variations in the WNT1 gene. The identification of a mutation in the WNT1 gene through NGS testing can confirm a diagnosis of OI type 15. It can also help in genetic counseling and family planning by providing information about the inheritance pattern and the risk of passing the condition on to future generations. Additionally, NGS testing can aid in the development of personalized treatment plans and potential targeted therapies for individuals with OI type 15.