Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves’ disease and 47, XXX in a woman: A case report
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DOI: 10.1097/md.0000000000031443
Abstract: Rationale: Coexistence of congenital adrenal hyperplasia due to 21-hydroxylase deficiency, Graves’ disease and 47, XXX is rare. We report a case of a 25-year-old woman presented with masculine appearance, hirsutism and enlarged clitoris. Lab tests… read more here.
Keywords: disease xxx; chromosome; hydroxylase deficiency; xxx ... See more keywords