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Alpha 1-antitrypsin deficiency and pregnancy.

作者信息

Kuller J A, Katz V L, McCoy M C, Bristow C L

机构信息

Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill 27599-7570, USA.

出版信息

Am J Perinatol. 1995 Sep;12(5):303-5. doi: 10.1055/s-2007-994480.

Abstract

Alpha1-antitrypsin deficiency is an inherited pulmonary disorder which results from a deficiency of a major plasma protease inhibitor. The onset and severity of symptoms vary widely and depend on the genotype and whether the patient smokes cigarettes. Alpha1-antitrypsin in pregnancy has only been previously reported twice. Our patient had a functional serum alpha1-antitrypsin level which was 15% of normal but was clinically asymptomatic and she did not smoke. Her genotype revealed a non-ZZ pattern. Her obstetric history was complicated by preterm labor in each of her five ongoing pregnancies. Alpha1-antitrypsin deficiency is inherited via two codominant autosomal genes. Although there is great variability in severity of disease, seriously affected patients may have emphysema and hepatic abnormalities. Patients with non-ZZ genotypes or who are heterozygotes may have favorable pregnancy outcomes.

摘要

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