Faed M J, Lamont M A, Baxby K
J Med Genet. 1982 Feb;19(1):49-56. doi: 10.1136/jmg.19.1.49.
Testicular biopsies from eight men with abnormal karyotypes have been examined for histological and cytogenetic evidence of disturbances of meiosis. Quantitative analysis of this material showed one, with a 13;14 Robertsonian translocation, to have apparently normal spermatogenesis. Three patients, one with a 47,XYY and two with 45,XY, inv 9 karyotypes, had an overall depression of spermatogenesis. Four others, all with major chromosomal abnormalities, had apparently normal spermatogenesis until the primary spermatocyte stage. Two of these had sex autosomal translocations. One, 45,Y,t(X;21), had a complete block at MI, the other, 46,X,t(Y;16), had a partial block at spermatid formation. One man with a reciprocal 2;10 translocation showed delay at all stages beyond spermatocyte formation and one man with an inversion of chromosome 3 showed impaired spermatid maturation.
对八名核型异常男性的睾丸活检组织进行了检查,以寻找减数分裂紊乱的组织学和细胞遗传学证据。对这些材料的定量分析显示,一名患有13;14罗伯逊易位的患者精子发生明显正常。三名患者,一名核型为47,XYY,两名核型为45,XY,inv 9,精子发生总体受到抑制。另外四名患者,均有主要染色体异常,在初级精母细胞阶段之前精子发生明显正常。其中两名患者有性染色体与常染色体易位。一名核型为45,Y,t(X;21)的患者在减数第一次分裂时完全受阻,另一名核型为46,X,t(Y;16)的患者在精子细胞形成时部分受阻。一名患有2;10相互易位的男性在精母细胞形成后的所有阶段都出现延迟,一名患有3号染色体倒位的男性精子细胞成熟受损。