Type: Respiratory / Genetic
Alpha-1 antitrypsin deficiency
An underdiagnosed genetic cause of lung and liver disease; augmentation therapy is available for selected patients.
Cystic Fibrosis
A multisystem autosomal-recessive disorder of the CFTR chloride channel; CFTR modulators have transformed outcomes for eligible genotypes.
Submit Your Paper to GMJ
No APC until January 2027.

