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EZH2 Gene Weaver Syndrome Genetic Test Cost

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

-21%

The EZH2 Gene Weaver Syndrome Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, aimed at detecting mutations in the EZH2 gene, which are closely associated with Weaver Syndrome. This condition is a rare genetic disorder characterized by accelerated growth and development, distinctive facial features, and other physical abnormalities. The test plays a crucial role in the early identification and management of the syndrome, allowing for tailored medical and supportive care plans to be developed for affected individuals.

Conducted through a blood sample or cheek swab, the test examines the DNA for specific mutations in the EZH2 gene that are indicative of Weaver Syndrome. The process is carried out in the state-of-the-art facilities of DNA Labs UAE, ensuring high accuracy and reliability of the results.

The cost of the EZH2 Gene Weaver Syndrome Genetic Test is set at 4400 AED, reflecting the advanced technology and expertise required to accurately identify the gene mutations. This investment can be invaluable for families seeking answers to developmental concerns in their children, providing them with crucial information for medical and developmental intervention strategies.

Description

EZH2 Gene Weaver Syndrome Genetic Test

Components: EZH2 Gene Weaver syndrome 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: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for EZH2 Gene Weaver syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EZH2 Gene Weaver syndrome NGS Genetic DNA Test gene EZH2.

Test Details: The EZH2 gene is associated with a condition called Weaver syndrome. Weaver syndrome is a rare genetic disorder characterized by overgrowth, advanced bone age, distinctive facial features, intellectual disability, and other developmental abnormalities. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the EZH2 gene and identify any mutations or variations that may be present. This type of testing allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of the individual’s genetic makeup. By identifying mutations or variations in the EZH2 gene, NGS genetic testing can help confirm a diagnosis of Weaver syndrome and provide information about the specific genetic changes involved. This information can be useful for genetic counseling, family planning, and management of the condition. It is important to note that NGS genetic testing is a complex process that requires specialized equipment and expertise. The test is typically performed on a blood or saliva sample and results can take several weeks to be reported. Additionally, the cost of NGS testing can vary depending on the specific laboratory and insurance coverage.

Test Name	EZH2 Gene Weaver syndrome 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 EZH2 Gene Weaver syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EZH2 Gene Weaver syndrome NGS Genetic DNA Test gene EZH2
Test Details	The EZH2 gene is associated with a condition called Weaver syndrome. Weaver syndrome is a rare genetic disorder characterized by overgrowth, advanced bone age, distinctive facial features, intellectual disability, and other developmental abnormalities. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the EZH2 gene and identify any mutations or variations that may be present. This type of testing allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of the individual’s genetic makeup. By identifying mutations or variations in the EZH2 gene, NGS genetic testing can help confirm a diagnosis of Weaver syndrome and provide information about the specific genetic changes involved. This information can be useful for genetic counseling, family planning, and management of the condition. It is important to note that NGS genetic testing is a complex process that requires specialized equipment and expertise. The test is typically performed on a blood or saliva sample and results can take several weeks to be reported. Additionally, the cost of NGS testing can vary depending on the specific laboratory and insurance coverage.