MID1 Gene Opitz G syndrome Genetic Test
Test Name: MID1 Gene Opitz G syndrome Genetic Test
Components: NGS Technology
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for MID1 Gene Opitz G syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MID1 Gene Opitz G syndrome.
Test Details
The MID1 gene is associated with a rare genetic disorder called Opitz G/BBB syndrome. Opitz G syndrome is characterized by a wide range of symptoms that can vary in severity, including craniofacial abnormalities, genitourinary defects, intellectual disability, and developmental delays.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Opitz G syndrome, NGS genetic testing can be used to identify mutations or variations in the MID1 gene, which is responsible for the syndrome.
NGS genetic testing is typically performed using a blood or saliva sample from the individual being tested. The sample is analyzed in a laboratory, where the DNA is sequenced and compared to a reference sequence. Any variations or mutations in the MID1 gene can then be identified and interpreted by geneticists or genetic counselors.
The results of NGS genetic testing for Opitz G syndrome can help confirm a diagnosis, guide medical management, provide information about the inheritance pattern, and offer reproductive options for affected individuals and their families.
It is important to note that genetic testing should be done under the guidance of a healthcare professional who specializes in genetics, as they can provide appropriate counseling and support throughout the testing process.
| Test Name | MID1 Gene Opitz G syndrome Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for MID1 Gene Opitz G syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MID1 Gene Opitz G syndrome |
| Test Details |
The MID1 gene is associated with a rare genetic disorder called Opitz G/BBB syndrome. Opitz G syndrome is characterized by a wide range of symptoms that can vary in severity, including craniofacial abnormalities, genitourinary defects, intellectual disability, and developmental delays. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Opitz G syndrome, NGS genetic testing can be used to identify mutations or variations in the MID1 gene, which is responsible for the syndrome. NGS genetic testing is typically performed using a blood or saliva sample from the individual being tested. The sample is analyzed in a laboratory, where the DNA is sequenced and compared to a reference sequence. Any variations or mutations in the MID1 gene can then be identified and interpreted by geneticists or genetic counselors. The results of NGS genetic testing for Opitz G syndrome can help confirm a diagnosis, guide medical management, provide information about the inheritance pattern, and offer reproductive options for affected individuals and their families. It is important to note that genetic testing should be done under the guidance of a healthcare professional who specializes in genetics, as they can provide appropriate counseling and support throughout the testing process. |
