FABRY DISEASE, QUANTITATIVE, BLOOD

  • Test Usage:
    Fabry disease is an X linked disorder caused by deficiency of the enzyme Alpha Galactosidase A due to mutations in GALA gene. Clinically the disease manifests with angiokeratomas, hypohidrosis, corneal & lens opacities and progressive small vessel disease of kidneys, heart & brain. Early initiation of enzyme therapy may prevent or slow the progression of life threatening complications.
  • Report Availability:
    Sample Daily by 4 pm; Report 4 Days
  • Sample Report:
44 Diagnostic Centers found for FABRY DISEASE, QUANTITATIVE, BLOOD in Allahabad