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[Mixed gonadal dysgenesis (MGD). Description of a case]
G Proto1, P Bartolomei, A Mazzolini
1Servizo di Endocrinologia, Ospedale Generale, Udine.
Minerva Endocrinologica
|October 1, 1991
Abstract:
The Authors report a case of mixed gonadal dysgenesis (DGM), with a mosaic karyotype consisting of two cell lines, one with 45 chromosomes and monosomic X (50%), the other with 46 chromosomes and one Y dicentric chromosome (50%). The patient presents a male phenotype, hypospadias (3rd degree), left cryptorchidism, hypotrophic right testis, short stature and a gonadal asymmetry.