GALACTOSEMIA PANEL 1

  • Test Usage:
    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%).
  • Report Availability:
    Sample Daily by 4 pm; Report 5 Days
  • Sample Report:
30 Diagnostic Centers found for GALACTOSEMIA PANEL 1 in Varanasi