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TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The “TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test” is a specialized diagnostic procedure aimed at identifying mutations in the TUBB3 gene, which are associated with a range of developmental brain abnormalities. This condition, known as Tubulinopathy, encompasses a spectrum of disorders that can lead to cortical dysplasia, a malformation of the brain cortex, among other neurological manifestations. These malformations can significantly impact brain function, leading to developmental delays, movement disorders, and epilepsy.

The test involves analyzing the patient’s DNA to look for specific genetic alterations in the TUBB3 gene that are known to cause these complex brain malformations. Early diagnosis through genetic testing can be crucial for the management of the condition, allowing for tailored treatment plans and interventions that can improve the quality of life for affected individuals.

Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test cost is set at 4400 AED. This investment covers the detailed analysis required to detect the presence of mutations in the TUBB3 gene, providing essential information for patients and their families. Through this test, DNA Labs UAE aims to offer hope and support to those facing the challenges associated with cortical dysplasia complex and other related brain malformations.

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TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test

Test Details

The TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test is a diagnostic test offered by DNA Labs UAE. This test utilizes Next Generation Sequencing (NGS) technology to analyze the DNA sequence of the TUBB3 gene. The TUBB3 gene is associated with a rare neurological disorder known as cortical dysplasia complex with other brain malformations type 1.

This disorder affects brain development and can lead to various symptoms including seizures, developmental delays, and intellectual disability. The NGS test for TUBB3 gene mutations can identify changes in the DNA sequence that may be responsible for the development of this disorder.

NGS technology allows for the rapid and accurate sequencing of large portions of the genome, enabling the identification of genetic variations that may be missed by traditional sequencing methods. This makes NGS an effective tool for diagnosing rare genetic disorders such as TUBB3 gene cortical dysplasia complex with other brain malformations type 1.

Test Components and Price

  • Test Name: TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test
  • Price: 4400.0 AED

Sample Condition and Report Delivery

The TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test requires a blood sample or extracted DNA. Alternatively, one drop of blood on an FTA card can also be used. The report will be delivered within 3 to 4 weeks.

Test Type and Doctor

This test falls under the category of Neurological Disorders and is conducted by a Neurologist in the Genetics department.

Pre Test Information

Prior to undergoing the TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a Genetic Counselling session is advised to draw a pedigree chart of family members affected with this disorder.

Conclusion

The NGS Genetic Test for TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 is a crucial tool for improving the diagnosis and management of this rare and complex neurological disorder. It enables the identification of genetic variations that may be responsible for the disorder’s development, allowing for confirmation of diagnosis, treatment guidance, and genetic counseling for affected individuals and their families.

Test Name TUBB3 Gene Cortical dysplasia complex with other brain malformations type 1 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 TUBB3 Gene Cortical dysplasia, complex, with other brain malformations, type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TUBB3 Gene Cortical dysplasia, complex, with other brain malformations, type 1
Test Details

NGS (Next Generation Sequencing) Genetic Test for TUBB3 Gene Cortical dysplasia, complex, with other brain malformations, type 1 is a diagnostic test that uses advanced genomic sequencing technology to analyze the DNA sequence of the TUBB3 gene. This gene is associated with a rare neurological disorder called cortical dysplasia, complex, with other brain malformations, type 1, which affects brain development and causes a range of symptoms, including seizures, developmental delays, and intellectual disability.

The NGS test for TUBB3 gene mutations can identify changes in the DNA sequence that may be responsible for the development of this disorder. This information can be used to confirm a diagnosis, guide treatment decisions, and provide genetic counseling to affected individuals and their families.

NGS technology allows for the rapid and accurate sequencing of large portions of the genome, enabling the identification of genetic variations that may be missed by traditional sequencing methods. This makes NGS an effective tool for diagnosing rare genetic disorders, such as TUBB3 gene cortical dysplasia, complex, with other brain malformations, type 1.

Overall, the NGS Genetic Test for TUBB3 Gene Cortical dysplasia, complex, with other brain malformations, type 1 is an important tool for improving the diagnosis and management of this rare and complex neurological disorder.