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真两性畸形由受精卵在细胞分裂过程中基因突变致性染色体异常而引起,很少见。我院收治2例,均经染色体核型分析、手术探查及病理切片证实。其中1例术后妊娠,更为少见。现报告如下,并简要讨论。临床资料 1984至1986年间,我院收治了2例真两性畸形,临床资料见附表。本组2例就诊时社会性别均为女性。例2在16岁前社会性别为男性,月经初潮后改为女性。心理性别为女性。畸形特点均为阴蒂
True hermaphroditism by the fertilized egg in the cell division process caused by genetic mutations caused by chromosomal abnormalities, is rare. Two cases were treated in our hospital, both by karyotype analysis, surgical exploration and pathology confirmed. One case of postoperative pregnancy, more rare. The report is as follows and briefly discussed. Clinical data 1984 to 1986, our hospital admitted to 2 cases of hermaphroditism, clinical data, see the attached table. The group of 2 cases were gender-based treatment of women. Example 2 Before the age of 16, the sex was male and changed to female after menarche. Psychological gender is female. Deformity characteristics are clitoris