Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/82377
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dc.contributor.authorValsalan, R.en
dc.contributor.authorZimmerman, A.en
dc.date.issued2013en
dc.identifier.citationInternal Medicine Journal, 2013; 43(3):334-337en
dc.identifier.issn1444-0903en
dc.identifier.issn1445-5994en
dc.identifier.urihttp://hdl.handle.net/2440/82377-
dc.description.abstractCongenital adrenal hyperplasia (CAH) is an uncommon condition. Its clinical presentation with hypertension is rare. Deficiency of the steroid 11-beta-hydroxylase accounts for less than 10% of CAH. We report a case of a 19-year-old patient who presents with hypertension with ambiguous genitalia secondary to adrenal steroidogenesis dysfunction. We also discuss the defects in adrenal steroidogenesis and clinical phenotypes of CAH.en
dc.description.statementofresponsibilityR. Valsalan and A. Zimmermannen
dc.language.isoenen
dc.publisherBlackwell Publishing Asiaen
dc.rights© 2013 The Authors.en
dc.subjectCongenital adrenal hyperplasia; 11-beta-hydroxylase deficiency; hypertensionen
dc.titleAmbiguous genitalia and hypertension in a patient with congenital adrenal hyperplasiaen
dc.typeJournal articleen
dc.identifier.rmid0020136087en
dc.identifier.doi10.1111/imj.12074en
dc.identifier.pubid15812-
pubs.library.collectionMedicine publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
Appears in Collections:Medicine publications

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