An Alpha-1 Antitrypsin Deficiency Screening Study in Patients with Chronic Obstructive Pulmonary Disease, Bronchiectasis, or Asthma in Turkey

PURPOSE: Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition characterized by decreased serum alpha-1 antitrypsin (AAT) levels. We aim to identify AATD in patients with chronic obstructive pulmonary disease (COPD), bronchiectasis, or asthma and to report the frequency of AAT variant...

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Detalles Bibliográficos
Autores principales: Tural Onur, Seda, Natoli, Antonino, Dreger, Bettina, Arınç, Sibel, Sarıoğlu, Nurhan, Çörtük, Mustafa, Karadoğan, Dilek, Şenyiğit, Abdurrahman, Yıldız, Birsen Pınar, Köktürk, Nurdan, Argun Barıs, Serap, Kodalak Cengiz, Sümeyye, Polatli, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693271/
https://www.ncbi.nlm.nih.gov/pubmed/38046982
http://dx.doi.org/10.2147/COPD.S425835

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693271/
https://www.ncbi.nlm.nih.gov/pubmed/38046982
http://dx.doi.org/10.2147/COPD.S425835

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