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ARX Gene Hydranencephaly with Abnormal Genitalia Lissencephaly X-Linked 2 Genetic Test

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

-21%

The ARX gene, known for its pivotal role in brain development and function, has been linked to a range of neurological disorders, including Hydranencephaly with Abnormal Genitalia and Lissencephaly X-Linked 2. These conditions are characterized by severe brain malformations and, in some cases, abnormalities in genital development. Hydranencephaly involves the replacement of the brain’s cerebral hemispheres with sacs filled with cerebrospinal fluid, while Lissencephaly X-Linked 2 is marked by a “smooth brain” due to abnormal neuronal migration, leading to intellectual disability and seizures.

To diagnose these conditions, genetic testing targeting the ARX gene can be instrumental. DNA Labs UAE offers a specialized genetic test for this purpose. The test aims to identify mutations in the ARX gene that are indicative of these disorders, providing crucial information for diagnosis, treatment planning, and genetic counseling. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to conduct such specialized genetic analysis. By opting for this test, individuals can gain valuable insights into their genetic makeup, empowering them with information that can guide medical and personal decision-making.

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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.