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[Seminoma and adrenogenital syndrome]
G Santoro1, F Nacchia, P Rocco
1Divisione di Chirurgia Generale, Universitá degli Studi Federico II, Napoli.
Il Giornale Di Chirurgia
|September 12, 1998
Abstract:
The Authors report a case of a 26 year old patient affected by adrenogenital syndrome, likely due to 21 hydroxylase defect, hermaphroditism (46XX genotype and female phenotype) and worked hyperandrogenism; moreover a hidden testis neoplasm (seminoma) was associated.