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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

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

Fig. 2

Documented G6PD deficient activity according to the identified G6PD patient genotypes (n = 81), with or without neonatal jaundice (NNJ). a Box and whisker plot genotypes with more than 3 affected individuals. No significant statistical differences were observed (p > 0.05); b Enzymatic activity documented in less than 3 affected individuals with corroborated G6PD genotypes. Filled triangles represent patients with NNJ, and open triangles are patients without NNJ

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172