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.

Operated by the Public Health Institute of Georgia (PHIG) · non-profit, ID 404407815 · 3 Betlemi Rise, Tbilisi 0105, Georgia · info@accreditation.ge · Policy Framework · Legal notice · Privacy · Accessibility · Part of the PHIG network