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支气管扩张症与少精子症:两个家族病例

Bronchiectasis and oligospermia: two families.

作者信息

Davis P B, Hubbard V S, Garvin A J

出版信息

Thorax. 1985 May;40(5):376-9. doi: 10.1136/thx.40.5.376.

Abstract

Five patients from two families had a bronchiectasis syndrome; the men also had oligospermia with poor progressive sperm motility. None of the patients had cystic fibrosis, alpha 1 antitrypsin deficiency, immunoglobulin deficiency, structural abnormalities of the bronchi, or abnormalities of ciliary ultrastructure. Onset of pulmonary symptoms was in the neonatal period or infancy, and bronchitis and bronchiectasis were most severe in the middle and lower lobes. Two patients had sinusitis and two otitis. The two men old enough to be studied had 2-10 X 10(6) sperm/ml of ejaculate with less than 10% progressively motile. There were no other associated anomalies. These patients probably had a distinct genetic error predisposing to pulmonary infection leading to bronchiectasis and, in men, oligospermia with poor progressive motility.

摘要

来自两个家族的5名患者患有支气管扩张综合征;这些男性还患有少精子症,精子进行性运动能力差。所有患者均无囊性纤维化、α1抗胰蛋白酶缺乏症、免疫球蛋白缺乏症、支气管结构异常或纤毛超微结构异常。肺部症状始于新生儿期或婴儿期,支气管炎和支气管扩张在中下叶最为严重。两名患者患有鼻窦炎,两名患有中耳炎。两名年龄足够接受研究的男性精液中精子浓度为2 - 10×10⁶/ml,进行性运动精子少于10%。无其他相关异常。这些患者可能存在一种独特的遗传缺陷,易导致肺部感染,进而引发支气管扩张,在男性中还会导致少精子症和精子进行性运动能力差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edcf/460070/5086b40b5a7d/thorax00233-0057-a.jpg

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