EXT2 Gene Exostoses multiple type 2 Genetic Test
Welcome to DNA Labs UAE, a leading genetic lab offering the EXT2 Gene Exostoses multiple type 2 Genetic Test. This blog post will provide you with detailed information about the test, including its components, cost, symptoms, and diagnosis process.
Test Details
The EXT2 gene is associated with a condition called multiple hereditary exostoses (MHE), also known as hereditary multiple osteochondromas. MHE is a rare genetic disorder characterized by the growth of multiple benign bone tumors called osteochondromas. These tumors typically develop on the long bones, such as the femur and tibia, as well as on the flat bones, such as the pelvis and scapula.
NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of MHE, an NGS genetic test can analyze the EXT2 gene, among other relevant genes, to identify any disease-causing mutations or variants.
By identifying mutations in the EXT2 gene, NGS testing can help confirm a diagnosis of MHE in individuals with suspected symptoms or a family history of the condition. This information can also be used for genetic counseling, family planning, and potentially guiding treatment decisions.
It’s important to note that NGS testing for EXT2 gene mutations is typically performed in specialized genetic testing laboratories and requires a healthcare professional’s order. The results of the test should be interpreted by a qualified healthcare provider or genetic counselor who can provide appropriate guidance and support.
Test Name: EXT2 Gene Exostoses multiple type 2 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
Prior to undergoing the EXT2 Gene Exostoses multiple type 2 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 with EXT2 Gene Exostoses, multiple, type 2 NGS Genetic DNA Test gene EXT2.
Conclusion
The EXT2 Gene Exostoses multiple type 2 Genetic Test offered by DNA Labs UAE is a valuable tool in diagnosing and managing multiple hereditary exostoses. By analyzing the EXT2 gene using NGS technology, this test can identify disease-causing mutations or variants, providing crucial information for genetic counseling and treatment decisions. If you suspect you or your family members may have MHE, consult with a healthcare professional to determine if the EXT2 Gene Exostoses multiple type 2 Genetic Test is right for you.
| Test Name | EXT2 Gene Exostoses multiple type 2 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 EXT2 Gene Exostoses, multiple, type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EXT2 Gene Exostoses, multiple, type 2 NGS Genetic DNA Test gene EXT2 |
| Test Details |
The EXT2 gene is associated with a condition called multiple hereditary exostoses (MHE), also known as hereditary multiple osteochondromas. MHE is a rare genetic disorder characterized by the growth of multiple benign bone tumors called osteochondromas. These tumors typically develop on the long bones, such as the femur and tibia, as well as on the flat bones, such as the pelvis and scapula. NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of MHE, an NGS genetic test can analyze the EXT2 gene, among other relevant genes, to identify any disease-causing mutations or variants. By identifying mutations in the EXT2 gene, NGS testing can help confirm a diagnosis of MHE in individuals with suspected symptoms or a family history of the condition. This information can also be used for genetic counseling, family planning, and potentially guiding treatment decisions. It’s important to note that NGS testing for EXT2 gene mutations is typically performed in specialized genetic testing laboratories and requires a healthcare professional’s order. The results of the test should be interpreted by a qualified healthcare provider or genetic counselor who can provide appropriate guidance and support. |
