Skip to main content
Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening

Fig. 1

Study algorithm. Infants with a positive newborn screening (NBS) test came from different primary care health centers. The clinical and biochemical approach of the 84 unrelated individuals initially referred to our center as G6PDd started with a new measurement of the G6PD activity in dried blood spots (DBS) and further G6PD genotyping experiments that unequivocally confirmed the G6PDd status in 81 patients, with or without neonatal jaundice (NNJ)

Back to article page

Orphanet Journal of Rare Diseases

ISSN: 1750-1172