Prevalence of genetic mutations in alpha-1 antitrypsin deficiency (aatd) in patients with chronic obstructive pulmonary disease in Colombia

BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) is an underrecognized genetic disorder associated mainly with pulmonary emphysema and Chronic Obstructive Pulmonary Disease (COPD). All individuals with COPD regardless of age or ethnicity should be tested for AATD, but in Colombia its prevalence in...

Descripción completa

Detalles Bibliográficos
Autores principales: Alí-Munive, Abraham, Leidy, Prada, Proaños, Nadia Juliana, Pedrozo-Pupo, John, Giraldo, Angela, Cano, Diana, Diaz-Bossa, Claudia, Mosquera, Ricardo, Paul, Hector, Gonzalez-García, Mauricio, Aguirre-Franco, Carlos, López-Campos, José Luis, Casas-Herrera, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158008/
https://www.ncbi.nlm.nih.gov/pubmed/37143026
http://dx.doi.org/10.1186/s12890-023-02453-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158008/
https://www.ncbi.nlm.nih.gov/pubmed/37143026
http://dx.doi.org/10.1186/s12890-023-02453-0

Ejemplares similares