Skip to content
My WebMD Sign In, Sign Up

Children's Health

Font Size

Galactosemia Test

Galactose is a sugar that is part of the lactose found in milk and milk products. A galactosemia test is a blood or urine test that checks for enzymes that are needed to change galactose into glucose, a sugar that your body uses for energy. A person with galactosemia doesn't have one of these enzymes, so high levels of galactose build up in the blood or urine.

When galactose builds up in a baby's blood, it can cause brain damage, seizures, and intellectual disabilities. The damage caused by galactosemia can begin within weeks after the baby has started drinking breast milk or formula. Babies with galactosemia need foods low in galactose in order to gain weight and to prevent brain damage, liver problems, infection, and cataracts.

Galactosemia is a rare disease that is passed from parents to children (inherited genetic disorder). A galactosemia test is usually done to determine whether a newborn has the disease. In a family with a member who has galactosemia, a genetic test can be done on adults to determine whether they have an increased chance of having a child with the disease.

Why It Is Done

A galactosemia test is done to:

  • Determine whether a newborn has the enzymes needed to change galactose into glucose.
  • Monitor the effectiveness of diet changes for a child with galactosemia.

How To Prepare

No special preparation is required before having this test.

Talk to your doctor about any concerns you have about the need for the test, its risks, how it will be done, or what the results will mean. To help you understand the importance of this test, fill out the medical test information formpdf(What is a PDF document?).

How It Is Done

Tests for galactosemia are done on a blood or urine sample.

Blood sample from a heel stick

If galactosemia testing is done on a baby, a heel stick will be done instead of a blood draw from a vein. For a heel stick blood sample, several drops of blood are collected from the heel of the baby. The skin of the heel is cleaned with alcohol and then punctured with a sterile lancet. Several drops of blood are collected inside circles on a specially prepared piece of paper. When enough blood has been collected, a gauze pad or cotton ball is placed over the puncture site. Pressure is maintained on the puncture site briefly to stop the bleeding, and then a small bandage is usually applied. A blood sample is usually collected within 2 to 3 days after birth.

If the test shows that the baby has galactosemia, the results will be confirmed on a blood sample taken from a vein.

Blood sample from a vein

WebMD Medical Reference from Healthwise

Last Updated: March 29, 2011
This information is not intended to replace the advice of a doctor. Healthwise disclaims any liability for the decisions you make based on this information.

Today in Children’s Health

preschool age girl sitting at desk
Article
look at my hand
Slideshow
 
woman with cleaning products
Slideshow
tissue box
Quiz
 

worried kid
fitArticle
boy on father's shoulder
Article
 
Child with red rash on cheeks
Slideshow
girl thinking
Article
 

babyapp
New
Child with adhd
Slideshow
 
rl with friends
fitSlideshow
Syringes and graph illustration
Tool
 
6-Week Challenges
Want to know more?
Eat Better Challenge - No diets here. One new healthy habit, one step at a time.
Get Up and Go Challenge - Get inspired and stay motivated.
Mood Boost Challenge - Fight the blahs, lower stress, and be happy.
I have read and agreed to WebMD's Privacy Policy.
Enter cell phone number
- -
Entering your cell phone number and pressing submit indicates you agree to receive text messages from WebMD related to this challenge. WebMD is utilizing a 3rd party vendor, CellTrust, to provide the messages. You can opt out at any time.
Standard text rates apply