Your browser doesn't support javascript.
loading
[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 en 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.
Asunto(s)
Search on Google
Banco de datos: MEDLINE Asunto principal: Enfisema Pulmonar / Deficiencia de alfa 1-Antitripsina / Enfermedad Pulmonar Obstructiva Crónica Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: Pl Año: 2004 Tipo del documento: Article
Search on Google
Banco de datos: MEDLINE Asunto principal: Enfisema Pulmonar / Deficiencia de alfa 1-Antitripsina / Enfermedad Pulmonar Obstructiva Crónica Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: Pl Año: 2004 Tipo del documento: Article