Autor: |
Kuca P; Oddziału Intensywnej Terapii Pneumonologiczno--Kardiologicznej, Warszawa., Kamiński D, Campbell E, Kołakowski J, Goljan-Geremek A, Puścińska E, Bieleń P, Nowiński A, Wojda E, Hawryłkiewicz I, Sliwiński P, Górecka D |
Jazyk: |
polština |
Zdroj: |
Pneumonologia i alergologia polska [Pneumonol Alergol Pol] 2004; Vol. 72 (9-10), pp. 420-3. |
Abstrakt: |
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. |
Databáze: |
MEDLINE |
Externí odkaz: |
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