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ZC4H2 Gene Wieacker-Wolff Syndrome Genetic Test Cost

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

-21%

The ZC4H2 gene plays a critical role in early neurological development, and mutations in this gene are associated with Wieacker-Wolff syndrome, a rare X-linked recessive disorder. This condition primarily affects males and is characterized by muscle weakness, developmental delays, and contractures, among other neurological and physical manifestations. Given the complexity and rarity of the syndrome, genetic testing for mutations in the ZC4H2 gene is a crucial tool for accurate diagnosis and understanding the condition’s inheritance pattern within families.

DNA Labs UAE offers a specialized genetic test aimed at detecting mutations in the ZC4H2 gene to confirm the diagnosis of Wieacker-Wolff syndrome. The test involves analyzing the patient’s DNA to identify specific mutations in the ZC4H2 gene that are known to cause the syndrome. This genetic test is an important step for affected families, as it aids in genetic counseling, management of the condition, and understanding the risk for future pregnancies.

The cost of the ZC4H2 Gene Wieacker-Wolff Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive analysis and the specialized expertise required to interpret the results accurately. For families facing the challenges of Wieacker-Wolff syndrome, this test provides essential information for managing the condition and planning for the future.

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ZC4H2 Gene Wieacker-Wolff Syndrome Genetic Test

Test Name: ZC4H2 Gene Wieacker-Wolff Syndrome Genetic Test

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

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 ZC4H2 Gene Wieacker-Wolff Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZC4H2 Gene Wieacker-Wolff Syndrome.

About ZC4H2 Gene Wieacker-Wolff Syndrome Genetic Test

The ZC4H2 gene is associated with a rare genetic disorder known as Wieacker-Wolff syndrome. This syndrome primarily affects males and is characterized by intellectual disability, muscle weakness, delayed speech development, and distinctive facial features.

NGS (Next-Generation Sequencing) is a type of genetic test that can analyze multiple genes simultaneously. In the context of Wieacker-Wolff syndrome, an NGS genetic test can be used to analyze the ZC4H2 gene for any mutations or variations that may be causing the syndrome. This test can help confirm a diagnosis and provide information about the specific genetic changes involved in the condition.

By identifying the specific genetic mutation causing Wieacker-Wolff syndrome, NGS testing can also help with genetic counseling and family planning decisions. Additionally, it may contribute to a better understanding of the underlying biology of the disorder, potentially leading to future therapeutic interventions.

Test Name ZC4H2 Gene Wieacker-Wolff syndrome 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 ZC4H2 Gene Wieacker-Wolff syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ZC4H2 Gene Wieacker-Wolff syndrome
Test Details

The ZC4H2 gene is associated with a rare genetic disorder known as Wieacker-Wolff syndrome. This syndrome primarily affects males and is characterized by intellectual disability, muscle weakness, delayed speech development, and distinctive facial features.

NGS (Next-Generation Sequencing) is a type of genetic test that can analyze multiple genes simultaneously. In the context of Wieacker-Wolff syndrome, an NGS genetic test can be used to analyze the ZC4H2 gene for any mutations or variations that may be causing the syndrome. This test can help confirm a diagnosis and provide information about the specific genetic changes involved in the condition.

By identifying the specific genetic mutation causing Wieacker-Wolff syndrome, NGS testing can also help with genetic counseling and family planning decisions. Additionally, it may contribute to a better understanding of the underlying biology of the disorder, potentially leading to future therapeutic interventions.

SKU: TEST-2112 Category:

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