Description

Galactosemia is an autosomal recessive disorder resulting from 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

Pre-Information

Avoid sample collection for 60 days post transfusion. Clinical and drug history must accompany sample.