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Gonadal Dysgenesis With a Familial Character
1966
Acta geneticae medicae et gemellologiae
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SummaryThe Authors report on a case of congenital anorchidism, confirmed by laparatomy, with negative sexual chromatin and an XY karyotype. One of his two sisters, with primary amenorrhea, presented marked hypoplasia of the genital tract, positive sexual chromatin and in 3% of the cells with 2 chromatine corpuscles, XO/XX/XXX karyotype. The presence in the same family of two cases of gonadal dysgenesis appears to have occurred by mere chance.
doi:10.1017/s1120962300014979
fatcat:f4kikv64yver7gzi3zzjr3oow4