EHMT1 Gene Kleefstra syndrome Genetic Test
Components: EHMT1 Gene Kleefstra syndrome 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: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for EHMT1 Gene Kleefstra syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EHMT1 Gene Kleefstra syndrome NGS Genetic DNA Test gene EHMT1
Test Details
The EHMT1 gene is associated with a rare genetic disorder called Kleefstra syndrome. Kleefstra syndrome is characterized by intellectual disability, developmental delay, speech and language impairments, and distinct facial features. NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the analysis of multiple genes simultaneously. It is commonly used to identify genetic variations and mutations that may be responsible for certain genetic disorders, including Kleefstra syndrome.
An NGS genetic test for Kleefstra syndrome involves sequencing the EHMT1 gene to identify any variations or mutations that may be present. This can help confirm a diagnosis of Kleefstra syndrome and provide valuable information for medical management and genetic counseling. It is important to note that genetic testing for Kleefstra syndrome, including NGS, is typically performed by medical professionals with expertise in genetics and genetic counseling. The results of the test should be interpreted by a healthcare provider who is knowledgeable about the specific disorder and its implications.
| Test Name | EHMT1 Gene Kleefstra 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 EHMT1 Gene Kleefstra syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EHMT1 Gene Kleefstra syndrome NGS Genetic DNA Test gene EHMT1 |
| Test Details |
The EHMT1 gene is associated with a rare genetic disorder called Kleefstra syndrome. Kleefstra syndrome is characterized by intellectual disability, developmental delay, speech and language impairments, and distinct facial features. NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the analysis of multiple genes simultaneously. It is commonly used to identify genetic variations and mutations that may be responsible for certain genetic disorders, including Kleefstra syndrome. An NGS genetic test for Kleefstra syndrome involves sequencing the EHMT1 gene to identify any variations or mutations that may be present. This can help confirm a diagnosis of Kleefstra syndrome and provide valuable information for medical management and genetic counseling. It is important to note that genetic testing for Kleefstra syndrome, including NGS, is typically performed by medical professionals with expertise in genetics and genetic counseling. The results of the test should be interpreted by a healthcare provider who is knowledgeable about the specific disorder and its implications. |
