COL11A2 Gene Fibrochondrogenesis 2 Genetic Test
Welcome to DNA Labs UAE, your trusted genetic lab in UAE. We offer the COL11A2 Gene Fibrochondrogenesis 2 Genetic Test to help diagnose and understand this rare genetic disorder.
Test Details
The COL11A2 gene is responsible for providing instructions for making a protein called type XI collagen. This protein is found in cartilage, which is the connective tissue that cushions and supports joints. Mutations in the COL11A2 gene can lead to a rare genetic disorder called fibrochondrogenesis 2.
Fibrochondrogenesis 2 is characterized by abnormal bone development, particularly in the long bones of the arms and legs. Affected individuals typically have short limbs, joint deformities, and a small chest. Other features may include a cleft palate, hearing loss, and abnormalities of the skull and facial bones.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes at the same time. It is a powerful tool for identifying genetic mutations and can be used to diagnose fibrochondrogenesis 2 by detecting mutations in the COL11A2 gene.
Test Name: COL11A2 Gene Fibrochondrogenesis 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 COL11A2 Gene Fibrochondrogenesis 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL11A2 Gene Fibrochondrogenesis 2 NGS Genetic DNA Test gene COL11A2.
If you suspect that you or your child may have fibrochondrogenesis 2, you should consult with a genetic counselor or a healthcare provider who can help guide you through the genetic testing process and interpret the results.
| Test Name | COL11A2 Gene Fibrochondrogenesis 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 COL11A2 Gene Fibrochondrogenesis 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL11A2 Gene Fibrochondrogenesis 2 NGS Genetic DNA Test gene COL11A2 |
| Test Details |
The COL11A2 gene is responsible for providing instructions for making a protein called type XI collagen. This protein is found in cartilage, which is the connective tissue that cushions and supports joints. Mutations in the COL11A2 gene can lead to a rare genetic disorder called fibrochondrogenesis 2. Fibrochondrogenesis 2 is characterized by abnormal bone development, particularly in the long bones of the arms and legs. Affected individuals typically have short limbs, joint deformities, and a small chest. Other features may include a cleft palate, hearing loss, and abnormalities of the skull and facial bones. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes at the same time. It is a powerful tool for identifying genetic mutations and can be used to diagnose fibrochondrogenesis 2 by detecting mutations in the COL11A2 gene. If you suspect that you or your child may have fibrochondrogenesis 2, you should consult with a genetic counselor or a healthcare provider who can help guide you through the genetic testing process and interpret the results. |
