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SLC5A1 Gene GlucoseGalactose malabsorption Genetic Test Cost

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

-21%

The SLC5A1 gene glucose-galactose malabsorption genetic test is a specialized diagnostic procedure designed to identify mutations in the SLC5A1 gene, which are responsible for glucose-galactose malabsorption (GGM). GGM is a rare genetic disorder that affects the body’s ability to absorb glucose and galactose, two important sugars, from the intestines. This condition can lead to severe dehydration, malnutrition, and failure to thrive if not diagnosed and managed properly.

The test involves analyzing the DNA to look for specific mutations in the SLC5A1 gene that are known to cause the disorder. It is a critical tool for confirming a suspected diagnosis of GGM, based on clinical symptoms and dietary response, and can also be used for carrier testing in families with a history of the condition.

Conducted at DNA Labs UAE, a leading genetic testing facility, the cost of the SLC5A1 gene glucose-galactose malabsorption genetic test is set at 4400 AED. The lab utilizes advanced genetic sequencing technologies to ensure accurate and reliable results, providing essential information for the management and treatment of affected individuals. This test is a vital resource for families and healthcare providers dealing with the challenges of glucose-galactose malabsorption, offering hope for better health outcomes through early and precise diagnosis.

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SLC5A1 Gene GlucoseGalactose malabsorption Genetic Test

Test Name: SLC5A1 Gene GlucoseGalactose malabsorption Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 SLC5A1 Gene Glucose/Galactose malabsorption NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Glucose/Galactose malabsorption.

Test Details

The SLC5A1 gene is responsible for encoding a protein called sodium/glucose cotransporter 1 (SGLT1). This protein is primarily found in the small intestine and is involved in the absorption of glucose and galactose from the diet into the bloodstream.

Glucose/galactose malabsorption is a genetic disorder characterized by the inability to absorb glucose and galactose from the diet. This condition is caused by mutations in the SLC5A1 gene, leading to a dysfunctional SGLT1 protein. As a result, affected individuals are unable to properly absorb glucose and galactose, leading to symptoms such as diarrhea, abdominal pain, and failure to thrive.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of glucose/galactose malabsorption, NGS genetic testing can be used to identify mutations in the SLC5A1 gene that may be causing the condition. This test can help confirm a diagnosis, guide treatment decisions, and provide information about the likelihood of passing on the condition to future generations.

Test Name SLC5A1 Gene GlucoseGalactose malabsorption 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 SLC5A1 Gene Glucose/Galactose malabsorption NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glucose/Galactose malabsorption
Test Details

The SLC5A1 gene is responsible for encoding a protein called sodium/glucose cotransporter 1 (SGLT1). This protein is primarily found in the small intestine and is involved in the absorption of glucose and galactose from the diet into the bloodstream.

Glucose/galactose malabsorption is a genetic disorder characterized by the inability to absorb glucose and galactose from the diet. This condition is caused by mutations in the SLC5A1 gene, leading to a dysfunctional SGLT1 protein. As a result, affected individuals are unable to properly absorb glucose and galactose, leading to symptoms such as diarrhea, abdominal pain, and failure to thrive.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of glucose/galactose malabsorption, NGS genetic testing can be used to identify mutations in the SLC5A1 gene that may be causing the condition. This test can help confirm a diagnosis, guide treatment decisions, and provide information about the likelihood of passing on the condition to future generations.

SKU: TEST-2343 Category:

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