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• W2085126974 abstract "A case of pure gonadal dysgenesis was investigated. The patient was an 18-year-old Japanese woman with a history of primary amenorrhea. She had poorly developed breasts, a hypoplastic uterus, a normal vagina and infantile genitalia. The patient's karyotype was 46,XYp-/ 47,XXYp-. Microsatellite analysis revealed that the X chromosomes of this patient originated from one of the two maternal X chromosomes. DNA analysis of the Y chromosome revealed that she had a deletion of SRY (the sex-determining region on the Y chromosome). She underwent laparoscopic gonadectomies with a final pathology consistent with gonadoblastoma. Laparoscopic surgery is recommended as it is much less invasive and associated with rapid postoperative recovery." @default.
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• W2085126974 date "2000-01-01" @default.
• W2085126974 modified "2023-10-02" @default.
• W2085126974 title "A Case of XY Pure Gonadal Dysgenesis with 46,XYp–/47,XXYp– Karyotype Whose Gonadoblastoma Was Removed Laparoscopically" @default.
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• W2085126974 doi "https://doi.org/10.1159/000010318" @default.
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