ARX Gene Hydranencephaly with abnormal genitaliaLissencephaly X-linked 2 Genetic Test
Components
- Test Name: ARX Gene Hydranencephaly with abnormal genitaliaLissencephaly X-linked 2 Genetic Test
- 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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for ARX Gene Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2 NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with ARX Gene Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2
Test Details
ARX Gene Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2 NGS Genetic Test is a type of genetic test that analyzes the ARX gene for specific mutations associated with Hydranencephaly with abnormal genitalia and Lissencephaly X-linked 2.
Hydranencephaly is a rare neurological condition characterized by the absence of the cerebral hemispheres (the outer part of the brain) and the presence of fluid-filled sacs in their place. This condition can lead to severe developmental delays and intellectual disabilities.
Lissencephaly X-linked 2, also known as XLAG syndrome, is a genetic disorder that affects brain development. It is characterized by the absence or underdevelopment of the folds and grooves (gyri and sulci) in the brain, leading to severe intellectual disability and developmental delays.
The ARX gene is responsible for providing instructions for the production of the Aristaless-related homeobox protein. Mutations in this gene can disrupt normal brain development and result in the aforementioned conditions.
The NGS (Next-Generation Sequencing) Genetic Test is a high-throughput sequencing technology that allows for the analysis of multiple genes simultaneously. This test can identify specific mutations or genetic variations in the ARX gene associated with Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2.
By identifying these genetic mutations, the test can provide a definitive diagnosis for individuals suspected to have Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2. This can help guide medical management, provide information on prognosis, and assist with genetic counseling for affected individuals and their families.
| Test Name | ARX Gene Hydranencephaly with abnormal genitaliaLissencephaly X-linked 2 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 ARX Gene Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ARX Gene Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2 |
| Test Details | ARX Gene Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2 NGS Genetic Test is a type of genetic test that analyzes the ARX gene for specific mutations associated with Hydranencephaly with abnormal genitalia and Lissencephaly X-linked 2. Hydranencephaly is a rare neurological condition characterized by the absence of the cerebral hemispheres (the outer part of the brain) and the presence of the fluid-filled sacs in their place. This condition can lead to severe developmental delays and intellectual disabilities. Lissencephaly X-linked 2, also known as XLAG syndrome, is a genetic disorder that affects brain development. It is characterized by the absence or underdevelopment of the folds and grooves (gyri and sulci) in the brain, leading to severe intellectual disability and developmental delays. The ARX gene is responsible for providing instructions for the production of the Aristaless-related homeobox protein. Mutations in this gene can disrupt normal brain development and result in the aforementioned conditions. The NGS (Next-Generation Sequencing) Genetic Test is a high-throughput sequencing technology that allows for the analysis of multiple genes simultaneously. This test can identify specific mutations or genetic variations in the ARX gene associated with Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2. By identifying these genetic mutations, the test can provide a definitive diagnosis for individuals suspected to have Hydranencephaly with abnormal genitalia/Lissencephaly X-linked 2. This can help guide medical management, provide information on prognosis, and assist with genetic counseling for affected individuals and their families. |
