CUL7 Gene Three M syndrome type 1 Genetic Test
Components:
- Test Name: CUL7 Gene Three M syndrome type 1 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 CUL7 Gene Three M syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CUL7 Gene Three M syndrome type 1 NGS Genetic DNA Test gene CUL7.
Test Details:
The CUL7 gene is associated with Three M syndrome type 1, which is a rare genetic disorder characterized by short stature, facial dysmorphism, and skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes to identify any variations or mutations that may be associated with a particular genetic disorder, such as Three M syndrome type 1. This test can help confirm a diagnosis, provide information about the specific genetic cause of the disorder, and guide treatment and management options.
Test Name | CUL7 Gene Three M syndrome type 1 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 CUL7 Gene Three M syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CUL7 Gene Three M syndrome type 1 NGS Genetic DNA Test gene CUL7 |
Test Details |
The CUL7 gene is associated with Three M syndrome type 1, which is a rare genetic disorder characterized by short stature, facial dysmorphism, and skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes to identify any variations or mutations that may be associated with a particular genetic disorder, such as Three M syndrome type 1. This test can help confirm a diagnosis, provide information about the specific genetic cause of the disorder, and guide treatment and management options. |