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ARX Gene Lissencephaly X-Linked Type 2 Genetic Test Cost

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

-21%

The ARX Gene Lissencephaly X-Linked Type 2 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the ARX gene, which are linked to Lissencephaly X-Linked Type 2, a rare genetic disorder. This condition is characterized by abnormal brain development that leads to smooth brain surfaces, intellectual disabilities, and seizures. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing it for specific genetic changes associated with the disorder.

The importance of this test lies in its ability to provide crucial information for families affected by Lissencephaly X-Linked Type 2, facilitating early intervention, management plans, and genetic counseling. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test ensures accuracy, confidentiality, and support through the diagnostic process. The cost of the ARX Gene Lissencephaly X-Linked Type 2 Genetic Test is 4400 AED, reflecting the comprehensive analysis and expert interpretation provided to diagnose this complex condition accurately.

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ARX Gene Lissencephaly X-linked type 2 Genetic Test

Test Name: ARX Gene Lissencephaly X-linked type 2 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 ARX Gene Lissencephaly, X-linked type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ARX Gene Lissencephaly, X-linked type 2 NGS Genetic DNA Test gene ARX

Test Details

ARX Gene Lissencephaly, X-linked type 2 NGS Genetic Test is a type of genetic test that analyzes the ARX gene for mutations associated with a specific type of lissencephaly called X-linked lissencephaly type 2. Lissencephaly is a rare genetic disorder characterized by the absence or underdevelopment of brain folds (gyri) and the presence of a smooth brain surface.

X-linked lissencephaly type 2 is caused by mutations in the ARX gene, which is located on the X chromosome. The NGS (Next-Generation Sequencing) genetic test involves sequencing the DNA of an individual to identify any mutations or variations in the ARX gene. This test can help in diagnosing X-linked lissencephaly type 2 and providing information about the specific mutation present in an affected individual.

Knowing the specific mutation can be helpful in understanding the severity of the condition, predicting the prognosis, and providing appropriate genetic counseling to affected individuals and their families. It is important to note that this genetic test is specifically designed to detect mutations in the ARX gene associated with X-linked lissencephaly type 2 and may not be suitable for diagnosing other types of lissencephaly or related disorders.

Genetic counseling and consultation with a healthcare professional are recommended before and after undergoing this test.

Test Name ARX Gene Lissencephaly X-linked type 2 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 ARX Gene Lissencephaly, X-linked type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ARX Gene Lissencephaly, X-linked type 2 NGS Genetic DNA Test gene ARX
Test Details

ARX Gene Lissencephaly, X-linked type 2 NGS Genetic Test is a type of genetic test that analyzes the ARX gene for mutations associated with a specific type of lissencephaly called X-linked lissencephaly type 2.

Lissencephaly is a rare genetic disorder characterized by the absence or underdevelopment of brain folds (gyri) and the presence of a smooth brain surface. X-linked lissencephaly type 2 is caused by mutations in the ARX gene, which is located on the X chromosome.

The NGS (Next-Generation Sequencing) genetic test involves sequencing the DNA of an individual to identify any mutations or variations in the ARX gene. This test can help in diagnosing X-linked lissencephaly type 2 and providing information about the specific mutation present in an affected individual.

Knowing the specific mutation can be helpful in understanding the severity of the condition, predicting the prognosis, and providing appropriate genetic counseling to affected individuals and their families.

It is important to note that this genetic test is specifically designed to detect mutations in the ARX gene associated with X-linked lissencephaly type 2 and may not be suitable for diagnosing other types of lissencephaly or related disorders. Genetic counseling and consultation with a healthcare professional are recommended before and after undergoing this test.

SKU: TEST-4214 Category:

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