KANSL1 Gene Koolen Syndrome Genetic Test
At DNA Labs UAE, we offer the KANSL1 Gene Koolen Syndrome Genetic Test for individuals suspected of having Koolen-de Vries syndrome. This rare genetic disorder is also known as Koolen syndrome or 17q21.31 microdeletion syndrome. Our comprehensive test includes the following details:
- Test Name: KANSL1 Gene Koolen Syndrome Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Test Type: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Before undergoing the KANSL1 Gene Koolen Syndrome Genetic Test, it is important 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 by Koolen syndrome.
Test Details
The KANSL1 gene is associated with Koolen-de Vries syndrome, a rare genetic disorder characterized by developmental delay, intellectual disability, distinctive facial features, and other physical abnormalities. Our NGS genetic testing method allows for the simultaneous analysis of multiple genes or the entire genome. This advanced sequencing technology provides a comprehensive view of an individual’s genetic makeup.
For Koolen syndrome, NGS genetic testing can identify mutations or deletions in the KANSL1 gene. This helps confirm a diagnosis and provides information about the specific genetic variant present in an individual. It can also be used for carrier testing in family members and prenatal testing for couples at risk of having a child with Koolen syndrome.
NGS genetic testing is a powerful tool in the field of genetics, providing valuable information for diagnosis, prognosis, and treatment planning for individuals with Koolen syndrome and their families.
| Test Name | KANSL1 Gene Koolen 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 | Dysmorphology |
| Doctor | Pediatrics |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for KANSL1 Gene Koolen syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KANSL1 Gene Koolen syndrome NGS Genetic DNA Test gene KANSL1 |
| Test Details |
The KANSL1 gene is associated with a rare genetic disorder called Koolen-de Vries syndrome, also known as Koolen syndrome or 17q21.31 microdeletion syndrome. This syndrome is characterized by developmental delay, intellectual disability, distinctive facial features, and other physical abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses advanced sequencing technologies to rapidly and accurately sequence DNA, providing a comprehensive view of an individual’s genetic makeup. In the context of Koolen syndrome, NGS genetic testing can be used to identify mutations or deletions in the KANSL1 gene. This can help confirm a diagnosis and provide information about the specific genetic variant present in an individual. It can also be used for carrier testing in family members and for prenatal testing in couples at risk of having a child with Koolen syndrome. NGS genetic testing is a powerful tool in the field of genetics and can provide valuable information for diagnosis, prognosis, and treatment planning for individuals with Koolen syndrome and their families. |
