本例Turner氏综合征染色体核型为46,xxp~-,在国内尚未见报道,现报告如下。患者女,32岁,已婚,工人,因患全身皮肤色素斑二年,伴有双膝关节肿痛一个月,于1983年12月17日入院。患者为足月顺产,但自幼就身材矮小,体质差,智力稍低。自15岁以后生长停滞。从未来过月经。结婚8年未生育。父母和兄妹5人均健在,发育正常。近两年来全身皮肤散在多形性暗褐色色素斑,稍发痒,以躯干和面颈部多见。1个 Turner’s syndrome chromosome karyotype in this case 46, xxp ~ -, has not been reported in the country, are as follows. Female patient, 32 years old, married, worker, suffering from systemic skin pigmentation for two years, accompanied by a double knee swelling and pain for a month, was December 17, 1983 admission. Patients with full-term birth, but since childhood, short stature, poor health, mental retardation. Growth has stalled since the age of 15. Never have menstruation. Married 8 years without childbirth. 5 parents and brother and sister are alive, normal development. Over the past two years the whole body scattered pleomorphic dark brown pigment spots, a little itchy to the trunk and face and neck more common. 1