Turner’s综合症又称先天性卵巢发育不全症,是一种较少见的遗传性症候群。此病于1938年由Turner首次发现,1959年由Ford等作细胞遗传学检查。据文献调查报导,每3000个活产婴儿中就有一例Turner’s综合症患者。她们常常以原发性闭经或第二性症不发育而求诊。现将我院最近诊断的六例Turner’s综合症的临床表现,细胞 Turner’s syndrome, also known as congenital ovarian hypoplasia, is a rare inherited syndrome. The disease was first discovered by Turner in 1938 and by cytogenetics in 1959 by Ford et al. According to the literature survey, Turner’s syndrome occurs in 1 in 3000 live births. They often seek treatment for primary amenorrhea or secondary sexual development. Now our hospital recently diagnosed six cases of Turner’s syndrome clinical manifestations of cells