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Galactosemia, Newborn Screen is a diagnostic test conducted shortly after birth to detect galactosemia, an inherited metabolic disorder. Galactosemia is characterized by the body's inability to metabolize galactose, a sugar in milk and dairy products. The newborn screen involves collecting a small blood sample from the baby's heel and analyzing it for elevated levels of galactose and its metabolites. Early detection through newborn screening is crucial as galactosemia can lead to severe health complications if left untreated, including liver damage, cognitive impairment, and cataracts. Positive results prompt further diagnostic testing and dietary interventions to manage the condition effectively from infancy.
| Test Name | Galactosemia, Newborn Screen Test |
| Also Known as | Neonatal Galactosemia Screening |
| Sample type | Blood |
| Preparation required. | No fasting required |
Sample to be collected
Blood
No special precaution required
The Ceruloplasmin Test price varies by city and healthcare provider, starting from ₹750 to ₹1460
Book a test at your preferred lab by selecting home sample collection
Get your sample collected by the lab technician at your home
Receive your lab reports within 24 hours over email
Where can I find a Galactosemia, Newborn Screen Test near me?
You can easily locate a diagnostic center offering the Galactosemia, Newborn Screen Test by visiting our website's "Lab" section and using the search feature to find the nearest lab in your area.
Can I book the Galactosemia, Newborn Screen Test for someone else?
Yes, you can book the Galactosemia, Newborn Screen Test for family members or others. You'll need to provide their basic details during the booking process.
How long does it take to get Galactosemia, Newborn Screen Test results?
Typically, Galactosemia, Newborn Screen Test results are available within 24-48 hours after sample collection. For certain specialized tests, it may take longer.