ANKRD11 Gene KBG syndrome Genetic Test
Components
- Test Name: ANKRD11 Gene KBG 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 ANKRD11 Gene KBG syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ANKRD11 Gene KBG syndrome NGS Genetic DNA Test gene ANKRD11.
Test Details
ANKRD11 is a gene that is associated with KBG syndrome, a rare genetic disorder characterized by distinctive facial features, intellectual disability, short stature, and skeletal abnormalities. The ANKRD11 gene provides instructions for making a protein that is involved in the development and function of various tissues and organs in the body.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. It allows for the detection of genetic variations or mutations in a more efficient and cost-effective manner compared to traditional sequencing methods.
A genetic test for KBG syndrome using NGS technology would involve sequencing the ANKRD11 gene to identify any potential mutations or variations that may be associated with the disorder. This can help in confirming a diagnosis of KBG syndrome and provide information about the specific genetic cause of the condition.
Genetic testing for KBG syndrome can be useful for individuals who have symptoms suggestive of the disorder or those with a family history of the condition. It can aid in providing a definitive diagnosis, guiding appropriate medical management, and offering genetic counseling to affected individuals and their families.
| Test Name | ANKRD11 Gene KBG 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 ANKRD11 Gene KBG syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ANKRD11 Gene KBG syndrome NGS Genetic DNA Test gene ANKRD11 |
| Test Details | ANKRD11 is a gene that is associated with KBG syndrome, a rare genetic disorder characterized by distinctive facial features, intellectual disability, short stature, and skeletal abnormalities. The ANKRD11 gene provides instructions for making a protein that is involved in the development and function of various tissues and organs in the body. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. It allows for the detection of genetic variations or mutations in a more efficient and cost-effective manner compared to traditional sequencing methods. A genetic test for KBG syndrome using NGS technology would involve sequencing the ANKRD11 gene to identify any potential mutations or variations that may be associated with the disorder. This can help in confirming a diagnosis of KBG syndrome and provide information about the specific genetic cause of the condition. Genetic testing for KBG syndrome can be useful for individuals who have symptoms suggestive of the disorder or those with a family history of the condition. It can aid in providing a definitive diagnosis, guiding appropriate medical management, and offering genetic counseling to affected individuals and their families. |
