TUBA1A Gene Lissencephaly type 3 Genetic Test
Test Details
The TUBA1A gene is associated with a rare brain development disorder called lissencephaly type 3. Lissencephaly is a condition characterized by smooth brain surface instead of the normal folded appearance. Lissencephaly type 3 specifically refers to a form of lissencephaly caused by mutations in the TUBA1A gene.
NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes at once. In the case of lissencephaly type 3, NGS genetic testing can be used to identify mutations in the TUBA1A gene. The test involves obtaining a DNA sample, typically through a blood sample, and sequencing the DNA to analyze the TUBA1A gene. The sequencing technology used in NGS allows for the detection of small changes or mutations in the gene that may be responsible for the development of lissencephaly type 3.
By identifying mutations in the TUBA1A gene, NGS genetic testing can provide a definitive diagnosis of lissencephaly type 3. This information can be important for understanding the cause of the condition, predicting the prognosis, and providing appropriate medical management and genetic counseling for affected individuals and their families.
Test Name: TUBA1A Gene Lissencephaly type 3 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 TUBA1A Gene Lissencephaly type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TUBA1A Gene Lissencephaly type 3 NGS Genetic DNA Test gene TUBA1A.
| Test Name | TUBA1A Gene Lissencephaly type 3 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 TUBA1A Gene Lissencephaly type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TUBA1A Gene Lissencephaly type 3 NGS Genetic DNA Test gene TUBA1A |
| Test Details | The TUBA1A gene is associated with a rare brain development disorder called lissencephaly type 3. Lissencephaly is a condition characterized by smooth brain surface instead of the normal folded appearance. Lissencephaly type 3 specifically refers to a form of lissencephaly caused by mutations in the TUBA1A gene. NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes at once. In the case of lissencephaly type 3, NGS genetic testing can be used to identify mutations in the TUBA1A gene. The test involves obtaining a DNA sample, typically through a blood sample, and sequencing the DNA to analyze the TUBA1A gene. The sequencing technology used in NGS allows for the detection of small changes or mutations in the gene that may be responsible for the development of lissencephaly type 3. By identifying mutations in the TUBA1A gene, NGS genetic testing can provide a definitive diagnosis of lissencephaly type 3. This information can be important for understanding the cause of the condition, predicting the prognosis, and providing appropriate medical management and genetic counseling for affected individuals and their families. |
