Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome

dc.creatorMacielGuerra, AT
dc.creatorGuerra, G
dc.creatorMarini, SHVL
dc.creatorBaptista, MTM
dc.creatorMarquesdeFaria, AP
dc.date1997
dc.dateMAY
dc.date2014-12-16T11:33:59Z
dc.date2015-11-26T17:01:49Z
dc.date2014-12-16T11:33:59Z
dc.date2015-11-26T17:01:49Z
dc.date.accessioned2018-03-28T23:49:44Z
dc.date.available2018-03-28T23:49:44Z
dc.identifierClinical Genetics. Munksgaard Int Publ Ltd, v. 51, n. 5, n. 351, n. 353, 1997.
dc.identifier0009-9163
dc.identifierWOS:A1997XE91800012
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/66850
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/66850
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/66850
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1278799
dc.descriptionWe report on a rare case of female pseudohermaphroditism due to classical 21-hydroxylase deficiency associated with Turner syndrome (45,X/46,XX). Difficulties in the management of both diseases are briefly discussed. We regard this rare combination as a coincidental occurrence.
dc.description51
dc.description5
dc.description351
dc.description353
dc.languageen
dc.publisherMunksgaard Int Publ Ltd
dc.publisherCopenhagen
dc.publisherDinamarca
dc.relationClinical Genetics
dc.relationClin. Genet.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectcongenital adrenal hyperplasia
dc.subjectfemale pseudohermaphroditism
dc.subjectTurner syndrome
dc.subjectAdrenal-hyperplasia
dc.titleFemale pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome
dc.typeArtículos de revistas


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