OBSL1 Gene Three M Syndrome Type 2 Genetic Test
Introduction
The OBSL1 gene is associated with a rare genetic disorder called Three M syndrome type 2. This disorder is characterized by short stature, facial dysmorphism, and skeletal abnormalities.
Test Details
The OBSL1 Gene Three M syndrome type 2 Genetic Test is a type of genetic testing that uses NGS (Next Generation Sequencing) technology to analyze multiple genes simultaneously. The test helps in identifying mutations or variations in the OBSL1 gene that may be responsible for the disorder.
Components
- Test Name: OBSL1 Gene Three M syndrome type 2 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 OBSL1 Gene Three M syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with OBSL1 Gene Three M syndrome type 2 NGS Genetic DNA Test gene OBSL1.
Benefits of the Test
By analyzing the patient’s DNA sample, NGS genetic testing can provide valuable information about the presence or absence of genetic mutations in the OBSL1 gene, helping to confirm a diagnosis of Three M syndrome type 2. This information can be useful for genetic counseling, family planning, and management of the condition.
Important Note
Genetic testing should always be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the test results.
| Test Name | OBSL1 Gene Three M syndrome type 2 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 OBSL1 Gene Three M syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with OBSL1 Gene Three M syndrome type 2 NGS Genetic DNA Test gene OBSL1 |
| Test Details |
The OBSL1 gene is associated with a rare genetic disorder called Three M syndrome type 2. This disorder is characterized by short stature, facial dysmorphism, and skeletal abnormalities. NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of Three M syndrome type 2, NGS genetic testing can be used to identify mutations or variations in the OBSL1 gene that may be responsible for the disorder. By analyzing the patient’s DNA sample, NGS genetic testing can provide valuable information about the presence or absence of genetic mutations in the OBSL1 gene, helping to confirm a diagnosis of Three M syndrome type 2. This information can be useful for genetic counseling, family planning, and management of the condition. It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the test results. |
