
G6PD Blood Test
G6PD Blood Test
Direct answer: This test detects Glucose-6-Phosphate Dehydrogenase deficiency that can cause red blood cell breakdown.
The Glucose-6-Phosphate Dehydrogenase (G6PD) Test measures G6PD enzyme activity, an essential enzyme that protects red blood cells from oxidative damage. A deficiency may lead to haemolytic anaemia, where red blood cells break down prematurely after infections, certain foods, or medications. This test supports early diagnosis of inherited enzyme disorders.
At healthcare nt sickcare, the G6PD test is available with home collection facility in Pune and direct walk-in testing at our Aundh centre. Samples are processed through NABL-accredited partner laboratories, providing reliable reports for patients across Pune, Maharashtra.
Who Should Consider This Test?
Direct answer: Individuals with unexplained anaemia, newborn jaundice, or family history of G6PD deficiency.
Doctors commonly recommend this test for infants with prolonged jaundice, patients with sudden anaemia after infections or medications, or before prescribing drugs known to trigger haemolysis.
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When should I do the G6PD test?
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Is fasting required before the G6PD test?
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Description
G6PD Blood Test
Direct answer: This test detects Glucose-6-Phosphate Dehydrogenase deficiency that can cause red blood cell breakdown.
The Glucose-6-Phosphate Dehydrogenase (G6PD) Test measures G6PD enzyme activity, an essential enzyme that protects red blood cells from oxidative damage. A deficiency may lead to haemolytic anaemia, where red blood cells break down prematurely after infections, certain foods, or medications. This test supports early diagnosis of inherited enzyme disorders.
At healthcare nt sickcare, the G6PD test is available with home collection facility in Pune and direct walk-in testing at our Aundh centre. Samples are processed through NABL-accredited partner laboratories, providing reliable reports for patients across Pune, Maharashtra.
Who Should Consider This Test?
Direct answer: Individuals with unexplained anaemia, newborn jaundice, or family history of G6PD deficiency.
Doctors commonly recommend this test for infants with prolonged jaundice, patients with sudden anaemia after infections or medications, or before prescribing drugs known to trigger haemolysis.











