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RUNX2 Gene Cleidocranial Dysplasia Genetic Test Cost

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

-21%

The RUNX2 Gene Cleidocranial Dysplasia Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the RUNX2 gene, which are associated with Cleidocranial Dysplasia (CCD). CCD is a rare genetic disorder characterized by abnormal development of the bones and teeth, notably delayed closure of the cranial sutures, underdeveloped or absent clavicles, and dental abnormalities. The RUNX2 gene plays a critical role in the development and differentiation of osteoblasts, the cells responsible for bone formation.

This genetic test is crucial for individuals showing symptoms of CCD or those with a family history of the condition, as it provides definitive genetic evidence of the disorder. Early diagnosis through genetic testing can guide appropriate management and treatment strategies, improving the quality of life for affected individuals.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the RUNX2 Gene Cleidocranial Dysplasia Genetic Test is 4400 AED. The price reflects the comprehensive analysis involved in detecting mutations within the RUNX2 gene and the expertise required to interpret the results accurately. For families and individuals undergoing this test, the information provided can be invaluable for making informed health and lifestyle decisions.

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RUNX2 Gene Cleidocranial Dysplasia Genetic Test

At DNA Labs UAE, we offer the RUNX2 Gene Cleidocranial Dysplasia Genetic Test. This test is designed to analyze the DNA sequence of the RUNX2 gene and detect any mutations or variations that may be present. Cleidocranial dysplasia (CCD) is a rare genetic disorder that affects the development of bones and teeth, and the RUNX2 gene is associated with this condition.

Test Components and Price

The price for the RUNX2 Gene Cleidocranial Dysplasia Genetic Test is 4400.0 AED. The test can be performed using blood or extracted DNA samples, or even just one drop of blood on an FTA card.

Report Delivery and Method

After the test is conducted, the report will be delivered within 3 to 4 weeks. We utilize Next-generation sequencing (NGS) technology for this genetic test. NGS allows for the rapid and cost-effective sequencing of large portions of the genome, making it an efficient tool for genetic testing.

Test Type and Doctor

The RUNX2 Gene Cleidocranial Dysplasia Genetic Test falls under the category of Osteology, Dermatology, and Immunology Disorders. The test is recommended to be conducted by a Dermatologist. The test is performed in our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the RUNX2 Gene Cleidocranial Dysplasia NGS Genetic DNA Test gene (RUNX2).

Test Details

The RUNX2 gene is associated with cleidocranial dysplasia (CCD), a rare genetic disorder that affects the development of bones and teeth. Next-generation sequencing (NGS) is a genetic test that can be used to analyze the DNA sequence of the RUNX2 gene and detect any mutations or variations that may be present. By performing an NGS genetic test for CCD, healthcare professionals can confirm a diagnosis, provide genetic counseling, and guide treatment options for individuals with the condition. This test can also be used for carrier screening in families with a history of CCD, allowing for early detection and prevention of the disorder in future generations.

Test Name RUNX2 Gene Cleidocranial dysplasia 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 RUNX2 Gene Cleidocranial dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RUNX2 Gene Cleidocranial dysplasia NGS Genetic DNA Test gene RUNX2
Test Details

The RUNX2 gene is associated with cleidocranial dysplasia (CCD), a rare genetic disorder that affects the development of bones and teeth. Next-generation sequencing (NGS) is a genetic test that can be used to analyze the DNA sequence of the RUNX2 gene and detect any mutations or variations that may be present.

NGS allows for the rapid and cost-effective sequencing of large portions of the genome, making it a valuable tool for genetic testing. In the case of CCD, NGS can identify specific mutations in the RUNX2 gene that are known to be associated with the disorder.

By performing an NGS genetic test for CCD, healthcare professionals can confirm a diagnosis, provide genetic counseling, and guide treatment options for individuals with the condition. Additionally, this test can also be used for carrier screening in families with a history of CCD, allowing for early detection and prevention of the disorder in future generations.

SKU: TEST-2889 Category:

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