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Alpha-1 antitrypsin deficiency, SZ phenotype: a rare type of a rare disease. Case report.

Pneumologia (Bucharest, Romania) - 1 Jan 2000

Nebunoiu Ana-Maria, Deleanu Oana Claudia, Rohan Ileana, Mihălţan Florin, Chorostowska-Wynimko Joanna, Ulmeanu Ruxandra

Abstract excerpt

Alpha-1 antitrypsin deficiency is one of the genetic diseases with a clear impact on the structure and function of the lung, rarely diagnosed and treated. We present the case of a 51-year-old female patient, heavy smoker, known with chronic obstructive pulmonary disease (COPD) for 12 years, untre...

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PMID: 25665366

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25665366-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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