[The variability of clinical presentation of chronic obstructive pulmonary disease in patients with hereditary alpha-1 antitrypsin deficiency]. / Zmiennosc obrazu klinicznego przewleklej obturacyjnej choroby pluc u chorych z wrodzonym niedoborem alfa-1 antytrypsyny.
Pneumonol Alergol Pol
; 72(9-10): 420-3, 2004.
Article
em Pl
| MEDLINE
| ID: mdl-16021998
ABSTRACT
Four patients with alpha-1 antitrypsin (alpha-1 AT) deficiency are presented one woman with severe (phenotype PiZ) and 3 men with moderate (phenotype PiMZ) deficiency of alpha-1 AT. The variability of clinical presentation of hereditary emphysema is described. In all patients tobacco smoking history, spirometric and 6-minutes walking tests as well as HRCT of the lung were performed and compared. The influence of smoking on the functional status is underlined.
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Base de dados:
MEDLINE
Assunto principal:
Enfisema Pulmonar
/
Deficiência de alfa 1-Antitripsina
/
Doença Pulmonar Obstrutiva Crônica
Idioma:
Pl
Ano de publicação:
2004
Tipo de documento:
Article