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. Author manuscript; available in PMC: 2017 Apr 12.
Published in final edited form as: Clin Genet. 2016 Jan 20;89(5):539–549. doi: 10.1111/cge.12711

Fig. 3.

Fig. 3

Clinical descriptors of our cohort capture the overlaps and distinctions among CF, CFTR-RD, and CRMS. Sweat chloride measurements are from the time point closest to diagnosis. CF, cystic fibrosis; CFTR-RD, cystic fibrosis transmembrane conductance regulator-related disorder; CRMS, CFTR-related metabolic syndrome; PI, pancreatic insufficient; PS, pancreatic sufficient.