The groups also showed a trend with regard to patient age ( Fig 2 ); G1 including the youngest patients (median, 1.08 years; IQR, 1.00–1.17), while G2 (median, 1.67 years; IQR, 1.20–1.96) and G3 (median, 4.09 years; IQR, 4.02–4.31) included increasingly older patients.
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Initial acquisition and succession of the cystic fibrosis lung microbiome is associated with disease progression in infants and preschool children.
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