Ørstavik Karen Helene
Rikshospitalet, Avdeling for medisinsk genetikk, 0027 Oslo.
Tidsskr Nor Laegeforen. 2008 Jan 31;128(3):324-6.
Male infertility is due to genetic factors in 15% of cases. Identification of genetic causes is important for both prognosis and treatment. The article gives an overview of the most frequent genetic causes of male infertility.
The article is based on literature retrieved through a search of Pubmed.
Klinefelter syndrome, 47, XXY, and microdeletion in AFZ (azoospermia factor) c on the long arm of the Y chromosome are the most common genetic causes of male infertility. Both are present in about 10-15% of males with azoospermia. Other important genetic causes are cystic fibrosis and androgen insensitivity syndrome. Men with azoospermia may become fathers using new reproductive techniques. The infertility may therefore be passed on to the next generation.
15%的男性不育病例是由遗传因素导致的。确定遗传病因对预后和治疗都很重要。本文概述了男性不育最常见的遗传病因。
本文基于通过检索PubMed获取的文献。
克兰费尔特综合征(47, XXY)以及Y染色体长臂上无精子症因子(azoospermia factor,AFZ)c区域的微缺失是男性不育最常见的遗传病因。在约10% - 15%的无精子症男性中都存在这两种情况。其他重要的遗传病因包括囊性纤维化和雄激素不敏感综合征。无精子症男性可通过新的生殖技术成为父亲。因此,不育问题可能会遗传给下一代。