17α-hydroxylase deficiency

Abstract

Objective: To search for molecular changes in two Argentinian sisters with a clinical and biochemical diagnosis of 17α-hydroxylase deficiency. Subjects: Both patients had 46 XX karyotype, with sexual infantilism, primary amenorrhea, and hypertension. Other member of the first degree family did not have this deficiency. Hormonal results: The patients showed… (More)
DOI: 10.1007/BF03260061

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