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GALT Gene Galactosemia Genetic Test Cost

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

-21%

The GALT Gene Galactosemia Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the GALT gene, which are responsible for a condition known as Galactosemia. Galactosemia is a rare genetic metabolic disorder that impairs the body’s ability to process and break down a simple sugar called galactose, leading to a range of health issues, including liver disease, cataracts, and intellectual disability if not treated early. The test is crucial for early detection and management of the condition, potentially preventing the onset of severe symptoms and complications. The cost of the GALT Gene Galactosemia Genetic Test at DNA Labs UAE is 4400 AED, making it an accessible option for individuals seeking comprehensive genetic screening in the region. By identifying the presence of specific mutations in the GALT gene, this test provides essential information for the diagnosis, treatment planning, and familial genetic counseling of Galactosemia.

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GALT Gene Galactosemia Genetic Test

Are you concerned about Galactosemia? DNA Labs UAE offers the GALT Gene Galactosemia Genetic Test to provide you with valuable information about this genetic disorder. Read on to learn more about the test, its components, cost, symptoms, diagnosis, and more.

Test Name: GALT Gene Galactosemia 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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information

Before undergoing the GALT Gene Galactosemia Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with Galactosemia.

Test Details

The GALT gene is responsible for producing an enzyme called galactose-1-phosphate uridylyltransferase. Galactosemia is a genetic disorder that occurs due to mutations in the GALT gene, resulting in a deficiency or complete absence of this enzyme. To diagnose galactosemia, a next-generation sequencing (NGS) genetic test is performed.

NGS technology allows for the simultaneous analysis of multiple genes, making it an efficient and comprehensive method for genetic testing. This test specifically analyzes the DNA sequence of the GALT gene to identify any mutations or variations that may be causing the disorder.

By identifying the specific mutations in the GALT gene, NGS genetic testing can confirm a diagnosis of galactosemia and help determine the severity of the condition. This information is crucial for managing the disorder and providing appropriate treatment and dietary restrictions to affected individuals.

If you suspect Galactosemia or have a family history of the disorder, consider getting the GALT Gene Galactosemia Genetic Test at DNA Labs UAE. Our experienced team and advanced technology ensure accurate results and personalized care. Contact us today to schedule an appointment.

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

The GALT gene is responsible for producing an enzyme called galactose-1-phosphate uridylyltransferase. Galactosemia is a genetic disorder that results from mutations in the GALT gene, leading to a deficiency or complete absence of this enzyme.

To diagnose galactosemia, a next-generation sequencing (NGS) genetic test can be performed. This test analyzes the DNA sequence of the GALT gene to identify any mutations or variations that may be causing the disorder. NGS technology allows for the simultaneous analysis of multiple genes, making it an efficient and comprehensive method for genetic testing.

By identifying the specific mutations in the GALT gene, NGS genetic testing can confirm a diagnosis of galactosemia and help determine the severity of the condition. This information is important for managing the disorder and providing appropriate treatment and dietary restrictions to affected individuals.

SKU: TEST-2331 Category:

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