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[Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency]
A Liotta1, M Cammarata, G Corsello
1Clinica Pediatrica I, Università di Palermo, Italia.
Abstract:
A case of male pseudohermaphroditism with adrenal failure and female external genitalia is described. The hormonal pattern and the clinical evolution of the patient are compatible to a partial 17 alpha hydroxylase deficiency.