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Chr. 11p15 Gene Beckwith-Wiedemann Syndrome Genetic Test Cost

Name: Chr. 11p15 Gene Beckwith-Wiedemann Syndrome Genetic Test Cost
SKU: TEST-4452
Price: 4400 AED
Availability: InStock

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

-21%

The Chr. 11p15 Gene Beckwith-Wiedemann Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the chromosome 11p15 region, which are associated with Beckwith-Wiedemann Syndrome (BWS). BWS is a congenital overgrowth disorder that can lead to an increased risk of childhood cancer and various other abnormalities, including macroglossia (enlarged tongue), abdominal wall defects, and hemihypertrophy (asymmetrical body growth).

This genetic test is crucial for early detection and management of BWS, as it allows for personalized monitoring and treatment plans to be developed, reducing the risk of complications associated with the syndrome. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed for specific genetic alterations in the 11p15 region that are indicative of BWS.

The cost of the Chr. 11p15 Gene Beckwith-Wiedemann Syndrome Genetic Test at DNA Labs UAE is 4400 AED. Given the complexity and the specialized nature of this test, it represents a significant step forward in the personalized care and management of individuals with Beckwith-Wiedemann Syndrome, offering families the information necessary to make informed health and treatment decisions.

Description

chr. 11p15 Gene Beckwith-Wiedemann syndrome Genetic Test

Test Name: chr. 11p15 Gene Beckwith-Wiedemann 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: Cancer

Doctor: Oncologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for chr. 11p15 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with chr. 11p15 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test gene chr. 11p15

Test Details: The chr. 11p15 gene refers to a specific region on chromosome 11 at position 15. This region contains several genes, including those associated with Beckwith-Wiedemann syndrome (BWS). Beckwith-Wiedemann syndrome is a rare genetic disorder characterized by overgrowth, specific facial features, and an increased risk of developing certain tumors. It is caused by alterations in genes located on chromosome 11p15, such as the CDKN1C and IGF2 genes.

NGS (Next-Generation Sequencing) is a high-throughput genetic testing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of Beckwith-Wiedemann syndrome, NGS can be used to identify genetic variations or mutations in the chr. 11p15 gene region that may be responsible for the disorder.

By performing an NGS genetic test for Beckwith-Wiedemann syndrome, healthcare professionals can determine if an individual has any genetic alterations in the chr. 11p15 gene region that are associated with the syndrome. This information can help with diagnosis, genetic counseling, and management of the condition.

Test Name	chr. 11p15 Gene Beckwith-Wiedemann 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	Cancer
Doctor	Oncologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for chr. 11p15 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with chr. 11p15 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test gene chr. 11p15
Test Details	The chr. 11p15 gene refers to a specific region on chromosome 11 at position 15. This region contains several genes, including those associated with Beckwith-Wiedemann syndrome (BWS). Beckwith-Wiedemann syndrome is a rare genetic disorder characterized by overgrowth, specific facial features, and an increased risk of developing certain tumors. It is caused by alterations in genes located on chromosome 11p15, such as the CDKN1C and IGF2 genes. NGS (Next-Generation Sequencing) is a high-throughput genetic testing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of Beckwith-Wiedemann syndrome, NGS can be used to identify genetic variations or mutations in the chr. 11p15 gene region that may be responsible for the disorder. By performing an NGS genetic test for Beckwith-Wiedemann syndrome, healthcare professionals can determine if an individual has any genetic alterations in the chr. 11p15 gene region that are associated with the syndrome. This information can help with diagnosis, genetic counseling, and management of the condition.