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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Incidental screen positive findings in a prospective cohort study in Matlab, Bangladesh: insights into expanded newborn screening for low-resource settings

Fig. 1

Frequency of screen positive determinations by sample type. CH, congenital hypothyroidism; SCID, severe combined immunodeficiency; GALT, galactosemia; IVA, isovaleric academia; HGB, hemoglobinopathy; BIOT, biotinidase deficiency; PKU, phenylketonuria; FAO, untargetted fatty acid oxidation disease; MCADD, medium chain acyl coA dehydrogenase deficiency; VLADD, very long chain acyl coA dehydrogenase deficiency

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172