Classical Galactosemia due to complete deficiency of Galactose 1 phosphate uridyltransferase is characterised by poor growth, mental retardation, speech abnormalities, vison impairment due to cataract and liver enlargement.Partial deficiency of Galactose 1 phosphate uridyltransferase leads to Galactosemia Duarte variant.
Sample Type - Blood
Reporting Time - 5 Days
Prerequisites - No special preparation required
Price - ₹2300/-
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