TCF4 Gene Pitt-Hopkins 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 TCF4 Gene Pitt-Hopkins syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCF4 Gene Pitt-Hopkins syndrome NGS Genetic DNA Test gene TCF4.
Test Details
The TCF4 gene is associated with Pitt-Hopkins syndrome, a rare genetic disorder characterized by intellectual disability, developmental delay, and distinctive facial features. Next-generation sequencing (NGS) genetic testing can be used to analyze the TCF4 gene and identify any mutations or variants that may be present.
NGS technology allows for the rapid and efficient sequencing of large amounts of DNA, enabling comprehensive analysis of multiple genes simultaneously. In the case of Pitt-Hopkins syndrome, NGS testing can help confirm a diagnosis by identifying specific changes in the TCF4 gene that are known to cause the disorder.
NGS genetic testing for Pitt-Hopkins syndrome typically involves collecting a blood or saliva sample from the individual undergoing testing. The DNA from the sample is then extracted and sequenced using NGS technology. The resulting data is analyzed to identify any mutations or variants in the TCF4 gene that may be associated with Pitt-Hopkins syndrome.
NGS testing can provide valuable information for individuals and families affected by Pitt-Hopkins syndrome, including confirmation of diagnosis, genetic counseling, and potential implications for treatment and management of the condition.
It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals with expertise in genetics.
| Test Name | TCF4 Gene Pitt-Hopkins 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 TCF4 Gene Pitt-Hopkins syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCF4 Gene Pitt-Hopkins syndrome NGS Genetic DNA Test gene TCF4 |
| Test Details |
The TCF4 gene is associated with Pitt-Hopkins syndrome, a rare genetic disorder characterized by intellectual disability, developmental delay, and distinctive facial features. Next-generation sequencing (NGS) genetic testing can be used to analyze the TCF4 gene and identify any mutations or variants that may be present. NGS technology allows for the rapid and efficient sequencing of large amounts of DNA, enabling comprehensive analysis of multiple genes simultaneously. In the case of Pitt-Hopkins syndrome, NGS testing can help confirm a diagnosis by identifying specific changes in the TCF4 gene that are known to cause the disorder. NGS genetic testing for Pitt-Hopkins syndrome typically involves collecting a blood or saliva sample from the individual undergoing testing. The DNA from the sample is then extracted and sequenced using NGS technology. The resulting data is analyzed to identify any mutations or variants in the TCF4 gene that may be associated with Pitt-Hopkins syndrome. NGS testing can provide valuable information for individuals and families affected by Pitt-Hopkins syndrome, including confirmation of diagnosis, genetic counseling, and potential implications for treatment and management of the condition. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals with expertise in genetics. |
