TUBG1 Gene Neurodevelopmental Malformation and Microcephaly Genetic Test
Welcome to DNA Labs UAE, where we offer advanced genetic testing services. In this blog post, we will be discussing the TUBG1 gene neurodevelopmental malformation and microcephaly genetic test.
Test Components and Price
The TUBG1 gene neurodevelopmental malformation and microcephaly genetic test is priced at 4400.0 AED. The test components include:
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Before undergoing the TUBG1 gene neurodevelopmental malformation and microcephaly 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 TUBG1 gene-related conditions.
Test Details
The TUBG1 gene is associated with neurodevelopmental malformations and microcephaly. Neurodevelopmental malformations refer to abnormalities in the development of the nervous system, which can lead to various neurological disorders. Microcephaly is a condition characterized by a smaller than average head size and is often associated with intellectual disabilities and developmental delays.
NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. It allows for the simultaneous analysis of multiple genes or even the entire genome, providing a comprehensive assessment of an individual’s genetic makeup.
In the case of TUBG1 gene-related conditions, NGS genetic testing can identify mutations or variations in the TUBG1 gene that may be contributing to the neurodevelopmental malformations and microcephaly. This type of genetic testing can be used for diagnostic purposes, helping to confirm a suspected genetic disorder in an individual. It can also be used for carrier testing, preimplantation genetic testing, or prenatal testing to assess the risk of passing on the TUBG1 gene mutation to future generations.
Overall, NGS genetic testing for the TUBG1 gene can provide valuable information for diagnosis, prognosis, and genetic counseling for individuals and families affected by neurodevelopmental malformations and microcephaly.
Test Name | TUBG1 Gene Neurodevelopmental malformation and microcephaly 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 TUBG1 Gene Neurodevelopmental malformation and microcephaly NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TUBG1 Gene Neurodevelopmental malformation and microcephaly |
Test Details |
The TUBG1 gene is associated with neurodevelopmental malformations and microcephaly. Neurodevelopmental malformations refer to abnormalities in the development of the nervous system, which can lead to various neurological disorders. Microcephaly, on the other hand, is a condition characterized by a smaller than average head size and is often associated with intellectual disabilities and developmental delays. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. It allows for the simultaneous analysis of multiple genes or even the entire genome, providing a comprehensive assessment of an individual’s genetic makeup. In the case of TUBG1 gene-related conditions, NGS genetic testing can identify mutations or variations in the TUBG1 gene that may be contributing to the neurodevelopmental malformations and microcephaly. NGS genetic testing can be used for diagnostic purposes, helping to confirm a suspected genetic disorder in an individual. It can also be used for carrier testing, preimplantation genetic testing, or prenatal testing to assess the risk of passing on the TUBG1 gene mutation to future generations. Overall, NGS genetic testing for the TUBG1 gene can provide valuable information for diagnosis, prognosis, and genetic counseling for individuals and families affected by neurodevelopmental malformations and microcephaly. |