Galactosemia GALT Gene Mutation Detection Test sale cost 1600 AED
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Galactosemia GALT Gene Mutation Detection Test Cost

Original price was: 2,150 د.إ.Current price is: 1,600 د.إ.

-26%

The “Galactosemia GALT Gene Mutation Detection Test” is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the GALT gene, which are responsible for galactosemia. Galactosemia is a genetic disorder that affects an individual’s ability to metabolize the sugar galactose properly. The condition can lead to various health issues, including liver damage, growth problems, and intellectual disabilities if not diagnosed and managed early.

This test is crucial for early detection, enabling timely intervention and management to mitigate the adverse effects of the disorder. By analyzing DNA samples, the test identifies specific mutations in the GALT gene that are indicative of galactosemia, providing essential information for healthcare providers to develop an appropriate treatment plan.

Offered at a cost of 1600 AED, the test at DNA Labs UAE represents a significant step forward in the genetic diagnosis and management of galactosemia, offering hope and improved outcomes for affected individuals and their families.

Home  Sample collection service available

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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GALACTOSEMIA GALT GENE MUTATION DETECTION Test

Test Name: GALACTOSEMIA GALT GENE MUTATION DETECTION Test

Components: Price: 1600.0 AED

Sample Condition: 4 mL (2 mL min.) whole blood from 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Report Delivery: Sample Daily by 11am; Report 15 days

Method: PCR Sequencing

Test type: Inborn Errors of Metabolism

Doctor: Pediatrician

Test Department: MOLECULAR DIAGNOSTICS

Pre Test Information: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Test Details

The GALACTOSEMIA (GALT) GENE MUTATION DETECTION test is a genetic test that is used to identify mutations in the GALT gene. This gene is responsible for producing an enzyme called galactose-1-phosphate uridylyltransferase, which is involved in the breakdown of galactose, a sugar found in milk and other dairy products.

Galactosemia is an inherited disorder that affects the body’s ability to break down galactose. If left untreated, it can lead to serious health problems, including liver damage, kidney problems, and intellectual disability. The GALT gene mutations are the most common cause of galactosemia.

The GALT gene mutation detection test involves analyzing a person’s DNA to identify any mutations or changes in the GALT gene. This can be done through various methods, such as DNA sequencing or targeted mutation analysis. The test can determine if a person carries mutations in the GALT gene, which can help diagnose galactosemia or determine if a person is a carrier of the condition.

The test is typically ordered for individuals who have symptoms of galactosemia or for those who have a family history of the condition. It can also be done for newborn screening purposes in some countries to identify infants who may have galactosemia. The results of the test can help guide treatment decisions and provide information about the risk of passing on the condition to future children.

Genetic counseling is often recommended for individuals who test positive for GALT gene mutations to discuss the implications of the results and to provide support and guidance.

Test Name GALACTOSEMIA GALT GENE MUTATION DETECTION Test
Components
Price 1600.0 AED
Sample Condition 4 mL (2 mL min.) whole blood from 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery Sample Daily by 11am;Report 15 days
Method PCR Sequencing
Test type Inborn Errors of Metabolism
Doctor Pediatrician
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

The GALACTOSEMIA (GALT) GENE MUTATION DETECTION test is a genetic test that is used to identify mutations in the GALT gene. This gene is responsible for producing an enzyme called galactose-1-phosphate uridylyltransferase, which is involved in the breakdown of galactose, a sugar found in milk and other dairy products.

Galactosemia is an inherited disorder that affects the body’s ability to break down galactose. If left untreated, it can lead to serious health problems, including liver damage, kidney problems, and intellectual disability. The GALT gene mutations are the most common cause of galactosemia.

The GALT gene mutation detection test involves analyzing a person’s DNA to identify any mutations or changes in the GALT gene. This can be done through various methods, such as DNA sequencing or targeted mutation analysis. The test can determine if a person carries mutations in the GALT gene, which can help diagnose galactosemia or determine if a person is a carrier of the condition.

The test is typically ordered for individuals who have symptoms of galactosemia or for those who have a family history of the condition. It can also be done for newborn screening purposes in some countries to identify infants who may have galactosemia.

The results of the test can help guide treatment decisions and provide information about the risk of passing on the condition to future children. Genetic counseling is often recommended for individuals who test positive for GALT gene mutations to discuss the implications of the results and to provide support and guidance.

SKU: TEST-5084