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VPS13B Gene Cohen Syndrome Genetic Test

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

-21%

The VPS13B Gene Cohen Syndrome Genetic Test is a specialized diagnostic examination designed to identify mutations in the VPS13B gene, which are responsible for causing Cohen Syndrome. This rare genetic disorder is characterized by developmental delay, intellectual disability, small head size (microcephaly), and distinctive facial features, among other symptoms. The test is a crucial tool for clinicians to accurately diagnose Cohen Syndrome, enabling appropriate management and support for affected individuals and their families.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test employs advanced genetic sequencing technologies to scrutinize the VPS13B gene for any abnormalities that are indicative of Cohen Syndrome. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the lab for the presence of mutations.

The cost of the VPS13B Gene Cohen Syndrome Genetic Test is set at 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the VPS13B gene. For families and individuals considering this test, it represents a significant step towards understanding and managing Cohen Syndrome, offering insights that can guide treatment decisions and support services.

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  • This test is not intended for medical diagnosis or treatment
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VPS13B Gene Cohen Syndrome Genetic Test

Cost: 4400.0 AED

Test Components:

  • 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:

A Genetic Counselling session is required to draw a pedigree chart of family members affected with VPS13B Gene Cohen syndrome.

Test Details:

The VPS13B gene is associated with Cohen syndrome, a rare genetic disorder characterized by developmental delay, intellectual disability, distinctive facial features, and vision problems.

NGS (Next-Generation Sequencing) genetic testing can identify mutations in the VPS13B gene that cause Cohen syndrome. This advanced technology analyzes a person’s DNA to detect changes in specific genes associated with genetic disorders.

NGS genetic testing for Cohen syndrome is beneficial for diagnosis, genetic counseling, and family planning. It provides valuable information for healthcare professionals to develop personalized treatment plans and support for individuals with this condition.

Test Name VPS13B Gene Cohen 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 VPS13B Gene Cohen syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with VPS13B Gene Cohen syndrome
Test Details

The VPS13B gene is associated with Cohen syndrome, which is a rare genetic disorder characterized by developmental delay, intellectual disability, distinctive facial features, and vision problems.

NGS (Next-Generation Sequencing) genetic testing can identify mutations in the VPS13B gene that cause Cohen syndrome. This type of testing uses advanced technology to analyze a person’s DNA and detect changes in specific genes associated with genetic disorders.

NGS genetic testing for Cohen syndrome can help with diagnosis, genetic counseling, and family planning. It can also provide valuable information for healthcare professionals to develop personalized treatment plans and support for individuals with this condition.