Use App for best experience!
Available for Android & iOS
Galactosemia is an autosomal recessive disorder resulting form the deficiency of any of the three enzymes required for galactose metabolism. Galactosemia due to deficiency of Galactose -1- phosphate uridyl transferase (GALT) is the commonest cause and is
Avoid sample collection for 60 days post transfusion. Clinical and drug history must accompany sample.