CenterWatch
  • Search Clinical Trials
  • Clinical Trial Listings
  • Volunteer
  • Learn About Clinical Trials

Classic Galactosemia

Classic Galactosemia is an inherited metabolic disorder that affects the body's ability to process galactose, a sugar found in milk and other dairy products. The condition is caused by a deficiency in the enzyme galactose-1-phosphate uridyltransferase (GALT) which leads to a buildup of toxic substances in the body. Symptoms of classic galactosemia can include vomiting, diarrhea, liver damage, developmental delays, and intellectual disability.

Entire World
Filters

Type

Distance
Age
0
0
Gender
Trial Phase
Sponsor

No Results Found

Sorry, there are no results for this search. Please try searching by condition, treatment or keyword

CenterWatch

5000 Centregreen Way, Suite 200
Cary, NC, 27513, USA

Phone: 703.538.7600
Toll Free: 888.838.5578

  • Disclaimer
  • Privacy Policy
  • Term of Use
  • Do Not Sell My Personal Information