精子減少,精少,精液減少,精液缺乏

Objective:To study the relation between severe oligospermia, azoospermia and abnormal chromosome karyotypes. 目的:探討男性嚴(yán)重少精子癥和無(wú)精子癥與染色體異常的關(guān)系。

FSH and LH in oligospermia were higher than in normal semen, but the differences were not significant (P>0.05). 少精癥組FSH、LH雖均較正常精液組高，但無(wú)顯著性意義（P>0.

Conclusion Mutation of Exon A in AR gene plays an important part in infertile men with oligospermia. 結(jié)論雄性激素受體基因外顯子A即基因轉(zhuǎn)錄激活區(qū)的突變是造成少精不育的重要原因。

The patients with oligospermia and asthnospermia, Group A was higher than group B in normal sperm morphology percent. 在少精組及弱精組中A組精子正常形態(tài)率高于B組，差異有統(tǒng)計(jì)學(xué)意義。

Conclusion: chromosomal abnormalities play an important role in oligospermia and azoospermia. 結(jié)論染色體異常是導(dǎo)致少、弱精子及無(wú)精子癥的重要因素之一。