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COL10A1 Gene Metaphyseal Chondrodysplasia Schmid Type Genetic Test Cost

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

-21%

The COL10A1 gene plays a crucial role in the development and maintenance of bones and cartilage in the human body. Mutations in this gene can lead to a condition known as Metaphyseal Chondrodysplasia, Schmid Type (MCDS), a rare genetic disorder characterized by skeletal abnormalities including short stature, bowed legs, and other deformities primarily affecting the long bones. The disorder stems from issues in the process of endochondral ossification, which is essential for the normal growth and development of bones.

To diagnose this condition, a genetic test targeting the COL10A1 gene can be performed. This test involves analyzing the DNA to identify mutations in the COL10A1 gene that are indicative of MCDS. It is a crucial step for confirming the diagnosis, understanding the severity of the condition, and guiding treatment and management strategies for affected individuals.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic testing service. The cost of the COL10A1 gene test for Metaphyseal Chondrodysplasia, Schmid Type, at DNA Labs UAE is 4400 AED. The test provides a comprehensive analysis of the COL10A1 gene to detect mutations associated with the condition, thereby facilitating early diagnosis and intervention. It is a valuable resource for families seeking answers about this rare genetic disorder and aiming for a better quality of life for those affected.

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COL10A1 Gene Metaphyseal Chondrodysplasia Schmid Type Genetic Test

At DNA Labs UAE, we offer the COL10A1 Gene Metaphyseal Chondrodysplasia Schmid Type Genetic Test. This test is designed to detect mutations in the COL10A1 gene, which is associated with metaphyseal chondrodysplasia, Schmid type.

Test Details

Metaphyseal chondrodysplasia, Schmid type is a rare genetic disorder characterized by short stature, bowed legs, and abnormalities in the growth plates of long bones. It is caused by mutations in the COL10A1 gene.

Our test utilizes NGS (Next-Generation Sequencing) technology, which allows for the analysis of multiple genes simultaneously. By analyzing the entire coding region of the COL10A1 gene, we can identify specific mutations or variants associated with metaphyseal chondrodysplasia, Schmid type.

Test Components and Price

The price of the COL10A1 Gene Metaphyseal Chondrodysplasia Schmid Type Genetic Test is 4400.0 AED.

Sample Condition

We accept blood samples or extracted DNA samples for this test. Alternatively, you can provide one drop of blood on an FTA card.

Report Delivery

Your test report will be delivered within 3 to 4 weeks from the date of sample submission.

Test Type

The COL10A1 Gene Metaphyseal Chondrodysplasia Schmid Type Genetic Test falls under the category of Osteology Dermatology Immunology Disorders.

Doctor and Test Department

This test is performed by a dermatologist and falls under the genetics department.

Pre Test Information

Prior to undergoing the COL10A1 Gene Metaphyseal Chondrodysplasia Schmid Type Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by COL10A1 Gene Metaphyseal Chondrodysplasia, Schmid type.

Importance of the Test

The information obtained from this test can help confirm a diagnosis, provide genetic counseling, and guide potential treatment options for individuals with metaphyseal chondrodysplasia, Schmid type. It is advised to consult with a healthcare professional or genetic counselor to determine if NGS genetic testing is appropriate for your situation and to discuss the potential benefits and limitations of the test.

Test Name COL10A1 Gene Metaphyseal chondrodysplasia Schmid type 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 COL10A1 Gene Metaphyseal chondrodysplasia, Schmid type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL10A1 Gene Metaphyseal chondrodysplasia, Schmid type NGS Genetic DNA Test gene COL10A1
Test Details

Metaphyseal chondrodysplasia, Schmid type is a rare genetic disorder characterized by short stature, bowed legs, and an abnormality in the growth plates of long bones. It is caused by mutations in the COL10A1 gene.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of specific genetic mutations or variants associated with a particular disorder. In the case of metaphyseal chondrodysplasia, Schmid type, NGS genetic testing can be used to detect mutations in the COL10A1 gene.

By analyzing the entire coding region of the COL10A1 gene, NGS testing can identify specific mutations that may be responsible for the development of the disorder. This information can help in confirming a diagnosis, providing genetic counseling, and guiding potential treatment options for individuals with metaphyseal chondrodysplasia, Schmid type.

It is important to consult with a healthcare professional or genetic counselor to determine if NGS genetic testing is appropriate and to discuss the potential benefits and limitations of the test.

SKU: TEST-3144 Category:

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