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. |