B9D1 Gene Meckel Syndrome Type 9 Genetic Test
At DNA Labs UAE, we offer the B9D1 Gene Meckel Syndrome Type 9 Genetic Test at a cost of AED 4400.0. This test is designed to diagnose Meckel syndrome type 9, a rare genetic disorder characterized by multiple malformations affecting various organs and systems in the body.
Test Components and Details
- Test Name: B9D1 Gene Meckel Syndrome Type 9 Genetic Test
- Price: AED 4400.0
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Hepatology, Nephrology, Endocrinology Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
Prior to undergoing the B9D1 Gene Meckel Syndrome Type 9 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the B9D1 gene. This information will aid in the accurate interpretation of the test results.
Understanding Meckel Syndrome Type 9
Meckel syndrome type 9 is a rare genetic disorder characterized by brain abnormalities, kidney cysts, polydactyly (extra fingers or toes), and other structural malformations. The B9D1 gene is associated with this syndrome. Our NGS genetic testing utilizes high-throughput technology to analyze multiple genes simultaneously. Specifically, it identifies mutations or variations in the B9D1 gene that may be responsible for Meckel syndrome type 9.
NGS Genetic Testing Process
NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any genetic variations or mutations. This process allows healthcare professionals to understand the underlying genetic cause of Meckel syndrome type 9 and provide important information for genetic counseling and management of the condition.
Please note that genetic testing for Meckel syndrome type 9 is typically conducted in specialized genetic laboratories. A referral from a healthcare professional with expertise in genetic disorders is required to undergo this test.
| Test Name | B9D1 Gene Meckel syndrome type 9 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 | Hepatology Nephrology Endocrinology Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for B9D1 Gene Meckel syndrome type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with B9D1 Gene Meckel syndrome type 9 NGS Genetic DNA Test gene B9D1 |
| Test Details | The B9D1 gene is associated with Meckel syndrome type 9, which is a rare genetic disorder characterized by multiple malformations affecting various organs and systems in the body. Meckel syndrome is typically characterized by brain abnormalities, kidney cysts, polydactyly (extra fingers or toes), and other structural malformations. NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of Meckel syndrome type 9, NGS genetic testing can be used to identify mutations or variations in the B9D1 gene that may be responsible for the disorder. This type of testing can help with the diagnosis of Meckel syndrome type 9 and provide information about the specific genetic variant involved. NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any genetic variations or mutations. This can help healthcare professionals understand the underlying genetic cause of a particular disorder and provide important information for genetic counseling and management of the condition. It’s important to note that genetic testing for Meckel syndrome type 9 is typically done in specialized genetic laboratories and requires a referral from a healthcare professional with expertise in genetic disorders. |
