COL5A1 Gene Ehlers-Danlos syndrome type 12 Genetic Test
Components: COL5A1 Gene Ehlers-Danlos syndrome type 12 Genetic Test
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 COL5A1 Gene Ehlers-Danlos syndrome type 1/2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL5A1 Gene Ehlers-Danlos syndrome type 1/2 NGS Genetic DNA Test gene COL5A1
Test Details: The COL5A1 gene is associated with Ehlers-Danlos syndrome type 1 and type 2. Ehlers-Danlos syndrome (EDS) is a group of genetic disorders that affect the connective tissues in the body. Type 1 and type 2 are both characterized by abnormalities in the structure and function of collagen, which is an important component of connective tissues. NGS (Next-Generation Sequencing) genetic testing is a type of DNA sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of Ehlers-Danlos syndrome, NGS genetic testing can be used to identify mutations or variations in the COL5A1 gene that may be responsible for the development of the condition. The purpose of this genetic test is to provide a definitive diagnosis of Ehlers-Danlos syndrome type 1 or type 2 by identifying specific genetic changes in the COL5A1 gene. This information can help healthcare professionals determine the most appropriate treatment and management strategies for individuals with this condition. It can also be useful for genetic counseling and family planning purposes. It’s important to note that genetic testing for Ehlers-Danlos syndrome is typically performed in individuals who have clinical symptoms consistent with the condition. The test is usually ordered by a healthcare professional with expertise in genetic disorders, such as a geneticist or a genetic counselor. The test may involve obtaining a blood sample or a saliva sample, which is then sent to a specialized laboratory for analysis. The results are typically interpreted by a geneticist or other qualified healthcare professional.
Test Name | COL5A1 Gene Ehlers-Danlos syndrome type 12 Genetic Test |
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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 COL5A1 Gene Ehlers-Danlos syndrome type 1/2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with COL5A1 Gene Ehlers-Danlos syndrome type 1/2 NGS Genetic DNA Test gene COL5A1 |
Test Details |
The COL5A1 gene is associated with Ehlers-Danlos syndrome type 1 and type 2. Ehlers-Danlos syndrome (EDS) is a group of genetic disorders that affect the connective tissues in the body. Type 1 and type 2 are both characterized by abnormalities in the structure and function of collagen, which is an important component of connective tissues. NGS (Next-Generation Sequencing) genetic testing is a type of DNA sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of Ehlers-Danlos syndrome, NGS genetic testing can be used to identify mutations or variations in the COL5A1 gene that may be responsible for the development of the condition. The purpose of this genetic test is to provide a definitive diagnosis of Ehlers-Danlos syndrome type 1 or type 2 by identifying specific genetic changes in the COL5A1 gene. This information can help healthcare professionals determine the most appropriate treatment and management strategies for individuals with this condition. It can also be useful for genetic counseling and family planning purposes. It’s important to note that genetic testing for Ehlers-Danlos syndrome is typically performed in individuals who have clinical symptoms consistent with the condition. The test is usually ordered by a healthcare professional with expertise in genetic disorders, such as a geneticist or a genetic counselor. The test may involve obtaining a blood sample or a saliva sample, which is then sent to a specialized laboratory for analysis. The results are typically interpreted by a geneticist or other qualified healthcare professional. |