Kuller J A, Katz V L, McCoy M C, Bristow C L
Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill 27599-7570, USA.
Am J Perinatol. 1995 Sep;12(5):303-5. doi: 10.1055/s-2007-994480.
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.
α1 - 抗胰蛋白酶缺乏症是一种遗传性肺部疾病,由主要血浆蛋白酶抑制剂缺乏引起。症状的发作和严重程度差异很大,取决于基因型以及患者是否吸烟。α1 - 抗胰蛋白酶在孕期的情况此前仅被报道过两次。我们的患者血清α1 - 抗胰蛋白酶功能水平仅为正常水平的15%,但临床上无症状,且她不吸烟。她的基因型显示为非ZZ型。她的产科病史较为复杂,在她正在进行的五次妊娠中每次都出现了早产。α1 - 抗胰蛋白酶缺乏症通过两个共显性常染色体基因遗传。尽管疾病严重程度差异很大,但严重受影响的患者可能患有肺气肿和肝脏异常。具有非ZZ基因型或为杂合子的患者可能有良好的妊娠结局。