FERMT1 Gene Kindler syndrome Genetic Test
At DNA Labs UAE, we offer the FERMT1 Gene Kindler syndrome Genetic Test for the diagnosis of Kindler syndrome. This test helps in identifying mutations or changes in the FERMT1 gene that are responsible for this rare genetic disorder.
Test Details
The FERMT1 gene is associated with Kindler syndrome, an inherited condition that affects the skin, causing it to be fragile and prone to blistering. It can also affect other organs and systems in the body.
Our FERMT1 Gene Kindler syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes or the entire genome. This comprehensive analysis enables more accurate diagnosis and personalized treatment plans.
Components and Price
The cost of the FERMT1 Gene Kindler syndrome Genetic Test is 4400.0 AED. The test can be performed on either blood or extracted DNA, or even one drop of blood on an FTA Card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The NGS technology is used to analyze the sample and detect any mutations or changes in the FERMT1 gene.
Test Type and Doctor
The FERMT1 Gene Kindler syndrome Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. It is conducted by dermatologists in our Genetics department.
Pre Test Information
Prior to undergoing the FERMT1 Gene Kindler syndrome Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with Kindler syndrome.
Importance of NGS Genetic Testing
NGS genetic testing is a powerful tool that provides a comprehensive analysis of an individual’s genetic makeup. It can accurately diagnose genetic disorders, identify carriers of genetic conditions, and offer valuable information for family planning.
If you suspect that you or someone you know may have Kindler syndrome, we recommend consulting with a healthcare professional or a genetic counselor. They can guide you through the process of undergoing NGS genetic testing and provide personalized advice based on the results.
| Test Name | FERMT1 Gene Kindler syndrome 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 FERMT1 Gene Kindler syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FERMT1 Gene Kindler syndrome NGS Genetic DNA Test gene FERMT1 |
| Test Details |
The FERMT1 gene is associated with a rare genetic disorder called Kindler syndrome. Kindler syndrome is an inherited condition that affects the skin, causing it to be fragile and prone to blistering. It can also affect other organs and systems in the body. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the case of Kindler syndrome, NGS genetic testing can be used to identify mutations or changes in the FERMT1 gene that are responsible for the condition. NGS genetic testing is a powerful tool that can provide a comprehensive analysis of an individual’s genetic makeup, allowing for more accurate diagnosis and personalized treatment plans. It can also help in identifying carriers of genetic conditions and providing information for family planning. If you suspect you or someone you know may have Kindler syndrome, consulting with a healthcare professional or a genetic counselor is recommended to discuss the possibility of undergoing NGS genetic testing. |
