Immunoglobulin G: A useful outcome marker in the follow‐up of cystic fibrosis patients?

Background and Methods Hypergammaglobulinemia (hyper‐IgG) and hypogammaglobulinemia (hypo‐IgG) have been reported in patients with cystic fibrosis (CF). Although the clinical respiratory course is paradoxically different, depending on the IgG status, this association remains elusive. Therefore, we p...

Ausführliche Beschreibung