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H19 Gene Beckwith-Wiedemann Syndrome Genetic Test Cost

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

-21%

The H19 Gene Beckwith-Wiedemann Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the H19 gene associated with Beckwith-Wiedemann Syndrome (BWS). BWS is a genetic disorder characterized by overgrowth and an increased risk of developing childhood tumors. The condition can lead to various clinical manifestations, including macroglossia, abdominal wall defects, and hemihyperplasia.

The test is conducted through a comprehensive analysis of the patient’s DNA to identify any genetic alterations in the H19 gene that may indicate the presence of Beckwith-Wiedemann Syndrome. This early detection is crucial for managing the condition, allowing for appropriate medical interventions and monitoring to mitigate the risks associated with the syndrome.

DNA Labs UAE offers this genetic test at a cost of 4400 AED. The test is performed by experienced geneticists and laboratory technicians using state-of-the-art technology to ensure accurate and reliable results. Patients opting for this test at DNA Labs UAE can expect a professional and supportive environment, with guidance provided throughout the testing process.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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H19 Gene Beckwith-Wiedemann syndrome Genetic Test

At DNA Labs UAE, we offer the H19 Gene Beckwith-Wiedemann syndrome Genetic Test for individuals suspected of having Beckwith-Wiedemann syndrome (BWS), a rare genetic disorder characterized by overgrowth, abdominal wall defects, an increased risk of childhood cancer, and other physical abnormalities.

Test Details

The H19 gene is associated with BWS. Our Next-generation sequencing (NGS) technology allows for the rapid and simultaneous sequencing of multiple genes or even the entire genome. In the context of BWS, NGS genetic testing refers to the analysis of the H19 gene using this advanced sequencing technology.

Test Components and Price

Test Name: H19 Gene Beckwith-Wiedemann syndrome Genetic Test
Components: NGS Technology
Price: 4400.0 AED

Sample Condition

Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery

3 to 4 Weeks

Test Type

Cancer

Doctor

Oncologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for H19 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with H19 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test gene H19.

Method

NGS Technology

Test Details

The H19 gene is associated with Beckwith-Wiedemann syndrome (BWS), a rare genetic disorder characterized by overgrowth, abdominal wall defects, an increased risk of childhood cancer, and other physical abnormalities. Next-generation sequencing (NGS) is a technology used for genetic testing that allows for the rapid and simultaneous sequencing of multiple genes or even the entire genome. In the context of BWS, NGS genetic testing refers to the analysis of the H19 gene using this advanced sequencing technology.

NGS genetic testing for BWS involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual suspected of having the disorder. The DNA is then sequenced using NGS technology to identify any mutations or abnormalities in the H19 gene. These mutations can help confirm a diagnosis of BWS and provide important information about the specific genetic cause of the disorder.

The results of the NGS genetic test for BWS can help guide medical management and provide information about the risk of developing certain complications associated with the disorder. Additionally, genetic testing can be useful for identifying family members who may also be at risk of having BWS or carrying the genetic mutation.

It is important to note that genetic testing for BWS, including NGS testing of the H19 gene, should be conducted and interpreted by a qualified geneticist or genetic counselor who specializes in the diagnosis and management of genetic disorders. They can provide guidance on the appropriate testing options, explain the implications of the results, and offer support and counseling for individuals and families affected by BWS.

Test Name H19 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 H19 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with H19 Gene Beckwith-Wiedemann syndrome NGS Genetic DNA Test gene H19
Test Details

The H19 gene is associated with Beckwith-Wiedemann syndrome (BWS), a rare genetic disorder characterized by overgrowth, abdominal wall defects, an increased risk of childhood cancer, and other physical abnormalities.

Next-generation sequencing (NGS) is a technology used for genetic testing that allows for the rapid and simultaneous sequencing of multiple genes or even the entire genome. In the context of BWS, NGS genetic testing refers to the analysis of the H19 gene using this advanced sequencing technology.

NGS genetic testing for BWS involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual suspected of having the disorder. The DNA is then sequenced using NGS technology to identify any mutations or abnormalities in the H19 gene. These mutations can help confirm a diagnosis of BWS and provide important information about the specific genetic cause of the disorder.

The results of the NGS genetic test for BWS can help guide medical management and provide information about the risk of developing certain complications associated with the disorder. Additionally, genetic testing can be useful for identifying family members who may also be at risk of having BWS or carrying the genetic mutation.

It is important to note that genetic testing for BWS, including NGS testing of the H19 gene, should be conducted and interpreted by a qualified geneticist or genetic counselor who specializes in the diagnosis and management of genetic disorders. They can provide guidance on the appropriate testing options, explain the implications of the results, and offer support and counseling for individuals and families affected by BWS.