The Galactose-1 Phosphate Uridyltransferase test in red blood cells (RBCs) detects the levels of the galactose-1 phosphate uridyltransferase enzyme in the blood. This enzyme is essential for galactose metabolism, helping to convert it into glucose.

Newborns: Especially in early screening programs for genetic disorders, to detect galactosemia cases. Children showing symptoms of galactose deficiency: Such as vomiting, diarrhea, growth delay, or behavioral changes. Families with a history of galactose metabolism disorders: As they may have a higher risk of the condition. Individuals with unexplained health issues: Such as growth delays or dietary problems. Individuals undergoing comprehensive health evaluations: As part of an integrated assessment of their overall health.

Frequent Vomiting: Especially after consuming galactose-containing foods. Diarrhea: Unexplained or persistent. Growth Delay: In weight or height. General Weakness or Fatigue: May be observed in the child. Feeding Problems: Such as refusal to eat or difficulty breastfeeding. Behavioral Changes: Such as irritability or lethargy. Visual or Hearing Problems: May develop due to galactose accumulation.

What is the purpose of this test? It is used to determine the levels of galactose-1 phosphate uridyltransferase enzyme, helping to diagnose enzyme deficiency and galactose metabolism disorders. How is the test performed? The test requires taking a blood sample, usually from red blood cells. How long does it take to get the results? Results typically take a few days to a week, depending on the laboratory. Does the test require special preparation? The test generally does not require special preparation, but it is advisable to consult the doctor regarding any specific instructions. What are the risks associated with the test? The risks are minimal and may include mild pain when the sample is taken. What do the test results mean? Low results indicate enzyme deficiency, which may require further testing or therapeutic guidance. Can medications affect the test results? Some medications may affect galactose metabolism, so it is recommended to inform the doctor about all medications and supplements being taken.

Normal levels of galactose-1 phosphate uridyltransferase in red blood cells may vary depending on the laboratory, but generally, normal values are around 4.0 to 15.0 international units per gram of hemoglobin (U/g Hb).

GALT Test for Infants in Saudi Arabia | Lahalak Platform

A vital test measuring the GALT enzyme responsible for converting galactose into energy, detecting early metabolic disorders in newborns to ensure healthy development.

Prices starts from: 264 SAR

Scientific name: Galactose-1 Phosphate Uridyltransferase (GALT) Test

The Galactose-1 Phosphate Uridyltransferase (GALT) test in red blood cells (RBCs) is a laboratory test used to measure the levels of the GALT enzyme in red blood cells. This enzyme is essential for galactose metabolism, playing a crucial role in converting galactose into glucose. The test is primarily used to diagnose enzyme deficiency conditions,...

Galactose-1 Phosphate Uridyltransferase (GALT) Test - GALT Metabolism Guard Test

Service type Laboratory test (Blood)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 264 SAR

Included Services

Galactose-1 Phosphate Uridyltransferase, RBCs Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

The Galactose-1 Phosphate Uridyltransferase test in red blood cells (RBCs) detects the levels of the galactose-1 phosphate uridyltransferase enzyme in the blood. This enzyme is essential for galactose metabolism, helping to convert it into glucose.

Recommended groups

Newborns: Especially in early screening programs for genetic disorders, to detect galactosemia cases.
Children showing symptoms of galactose deficiency: Such as vomiting, diarrhea, growth delay, or behavioral changes.
Families with a history of galactose metabolism disorders: As they may have a higher risk of the condition.
Individuals with unexplained health issues: Such as growth delays or dietary problems.
Individuals undergoing comprehensive health evaluations: As part of an integrated assessment of their overall health.

Symptoms indicative

Frequent Vomiting: Especially after consuming galactose-containing foods.
Diarrhea: Unexplained or persistent.
Growth Delay: In weight or height.
General Weakness or Fatigue: May be observed in the child.
Feeding Problems: Such as refusal to eat or difficulty breastfeeding.
Behavioral Changes: Such as irritability or lethargy.

FAQs

What is the purpose of this test? It is used to determine the levels of galactose-1 phosphate uridyltransferase enzyme, helping to diagnose enzyme deficiency and galactose metabolism disorders.
How is the test performed? The test requires taking a blood sample, usually from red blood cells.
How long does it take to get the results? Results typically take a few days to a week, depending on the laboratory.
Does the test require special preparation? The test generally does not require special preparation, but it is advisable to consult the doctor regarding any specific instructions.
What are the risks associated with the test? The risks are minimal and may include mild pain when the sample is taken.
What do the test results mean? Low results indicate enzyme deficiency, which may require further testing or therapeutic guidance.

Normal Levels

Normal levels of galactose-1 phosphate uridyltransferase in red blood cells may vary depending on the laboratory, but generally, normal values are around 4.0 to 15.0 international units per gram of hemoglobin (U/g Hb).