GALACTOSEMIA PANEL 1
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 called Classical Galactosemia. Duarte variant galactosemia is generally associated with higher levels of enzyme activity (5-20%) than Classical galactosemia (< 5%).
Parameter(s) covered : 3
Report Frequency: Sample Daily by 4 pm; Report 5 days
Special Instruction: Avoid sample collection for 60 days post transfusion. Clinical and drug history must accompany sample.
Price : ₹ 2600.00
Parameters
- GALACTOSEMIA SCREENING
- Control value
- Patient value