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GBA Gene Gaucher disease type 3 Genetic Test Cost

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

-21%

The GBA Gene Gaucher Disease Type 3 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the GBA gene which are responsible for Gaucher Disease Type 3. This condition is a rare, inherited metabolic disorder where a specific type of fat called glucocerebroside accumulates in various body tissues, affecting their function. Type 3 Gaucher Disease, also known as the chronic neuronopathic form, presents with systemic symptoms as well as neurological complications.

The genetic test involves analyzing the patient’s DNA to look for mutations in the GBA gene, which provides instructions for producing the enzyme glucocerebrosidase. This enzyme is crucial for breaking down glucocerebroside. Mutations in the GBA gene lead to reduced activity of this enzyme, causing the accumulation of glucocerebroside.

This test is critical for the early diagnosis of Gaucher Disease Type 3, enabling timely intervention and management of the condition. It is also valuable for carrier screening and prenatal diagnosis, providing essential information for families with a history of the disease.

The cost of the GBA Gene Gaucher Disease Type 3 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the GBA gene.

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GBA Gene Gaucher disease type 3 Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab in the UAE. We offer the GBA Gene Gaucher disease type 3 Genetic Test at a cost of AED 4400.0.

Test Details

The GBA gene Gaucher disease type 3 NGS genetic test is a diagnostic test used to detect mutations in the GBA gene that are associated with Gaucher disease type 3. Gaucher disease is a rare genetic disorder characterized by the accumulation of a fatty substance called glucocerebroside in certain organs and tissues, primarily the spleen, liver, and bone marrow.

This test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the GBA gene and identify any mutations or changes that may be present. It can detect both common and rare mutations in the GBA gene that are associated with Gaucher disease type 3.

Gaucher disease type 3 is a more severe form of Gaucher disease that typically presents in childhood. It is characterized by neurological symptoms in addition to the organ and tissue involvement seen in other types of Gaucher disease.

Early detection and diagnosis through genetic testing can help guide treatment and management strategies for individuals with Gaucher disease type 3.

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: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the GBA Gene Gaucher disease type 3 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with Gaucher disease type 3.

By gathering this information, we can better understand the patient’s genetic background and make informed decisions regarding their healthcare.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our team of experienced professionals, including general physicians and geneticists, are dedicated to helping individuals and families affected by genetic disorders.

Test Name GBA Gene Gaucher disease type 3 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GBA Gene Gaucher disease type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Gaucher disease type 3
Test Details

The GBA gene Gaucher disease type 3 NGS genetic test is a diagnostic test used to detect mutations in the GBA gene that are associated with Gaucher disease type 3. Gaucher disease is a rare genetic disorder characterized by the accumulation of a fatty substance called glucocerebroside in certain organs and tissues, primarily the spleen, liver, and bone marrow.

This test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the GBA gene and identify any mutations or changes that may be present. It can detect both common and rare mutations in the GBA gene that are associated with Gaucher disease type 3.

Gaucher disease type 3 is a more severe form of Gaucher disease that typically presents in childhood. It is characterized by neurological symptoms in addition to the organ and tissue involvement seen in other types of Gaucher disease. Early detection and diagnosis through genetic testing can help guide treatment and management strategies for individuals with Gaucher disease type 3.

SKU: TEST-2336 Category:

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