Consistent with previously published reports, there was a high prevalence of subjects with one CF-causing mutation and a second mutation known to be associated with variable penetrance for CF and CFTR-RD such as D1152H and R117H.[28–30] A study of CF patients with one copy of D1152H and another CF-causing mutation has shown low incidence of symptoms in childhood, but up to 70% of adults have bronchiectasis.[29] Though this may be biased towards severe cases referred to CF centers, it illustrates the potential of these mutations to produce a pathologic phenotype that may be able to be averted. The gene discussed is CFTR; the disease is bronchiectasis.