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dc.contributor.authorStuchi-Perez, Eliana G.-
dc.contributor.authorHackel, Christine-
dc.contributor.authorOliveira, Luiz Eduardo C.-
dc.contributor.authorFerraz, Lucio F. C.-
dc.contributor.authorOliveira, Laurione C.-
dc.contributor.authorNunes-Silva, Daniela-
dc.contributor.authorToralles, Maria Betania-
dc.contributor.authorSteinmetz, Leandra-
dc.contributor.authorDamiani, Durval-
dc.contributor.authorMaciel-Guerra, Andrea T.-
dc.contributor.authorGuerra Júnior, Gil-
dc.date.accessioned2014-05-27T11:21:42Z-
dc.date.accessioned2016-10-25T18:21:28Z-
dc.date.available2014-05-27T11:21:42Z-
dc.date.available2016-10-25T18:21:28Z-
dc.date.issued2005-12-01-
dc.identifierhttp://dx.doi.org/10.1515/JPEM.2005.18.12.1383-
dc.identifier.citationJournal of Pediatric Endocrinology and Metabolism, v. 18, n. 12, p. 1383-1389, 2005.-
dc.identifier.issn0334-018X-
dc.identifier.urihttp://hdl.handle.net/11449/68561-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68561-
dc.description.abstractAim: To evaluate anti-Müllerian hormone (AMH) levels in patients with clinical and molecular diagnosis of 5α-reductase 2 deficiency. Patients and methods: Data from 14 patients whose age ranged from 21 days to 29 years were analyzed according to age and pubertal stage. Sexual ambiguity was rated as Prader III in 11 patients. LH, FSH, testosterone (T), dihydrotestosterone (DHT) and AMH serum levels were measured in all but two patients, who had been previously submitted to gonadectomy; T and DHT were also measured in 20 age-matched controls. Results: Gonadotropin levels were normal in all but one patient who retained gonads (six of whom had reached puberty) and T/DHT ratio was elevated in all patients when compared to controls. All prepubertal patients had AMH levels < -1 SD for age, while most pubertal patients had AMH levels compatible with pubertal stage. Conclusions: Prepubertal patients with 5α-reductase 2 deficiency have AMH values in the lower part of the normal range. These data indicate that T does not need to be converted to DHT to inhibit AMH secretion by Sertoli cells. © Freund Publishing House Ltd., London.en
dc.format.extent1383-1389-
dc.language.isoeng-
dc.sourceScopus-
dc.subject5α-reductase-
dc.subjectAndrogen insensitivity syndrome-
dc.subjectDihydrotestosterone-
dc.subjectMüllerian inhibiting hormone-
dc.subjectPseudohermaphroditism-
dc.subjectTestosterone-
dc.subjectandrostanolone-
dc.subjectglycoprotein-
dc.subjectmullerian inhibiting hormone-
dc.subjectmullerian-inhibiting hormone-
dc.subjectsteroid 5alpha reductase-
dc.subjecttestis peptide hormone-
dc.subjecttestosterone-
dc.subjectandrogen receptor-
dc.subjectchorionic gonadotropin-
dc.subjectfollitropin-
dc.subjectluteinizing hormone-
dc.subjectMuellerian inhibiting factor-
dc.subjectadolescent-
dc.subjectadult-
dc.subjectblood-
dc.subjectcase control study-
dc.subjectchild-
dc.subjectfemale-
dc.subjectgenetics-
dc.subjecthuman-
dc.subjectinfant-
dc.subjectmale-
dc.subjectnewborn-
dc.subjectorchiectomy-
dc.subjectphysiology-
dc.subjectpreschool child-
dc.subjectage distribution-
dc.subjectclinical article-
dc.subjectcontrolled study-
dc.subjectgonadectomy-
dc.subjectgonadotropin blood level-
dc.subjecthormonal regulation-
dc.subjecthormone action-
dc.subjecthormone blood level-
dc.subjecthormone determination-
dc.subjecthormone release-
dc.subjectprepuberty-
dc.subjectprotein deficiency-
dc.subjectpseudohermaphroditism-
dc.subjectpuberty-
dc.subjectsexual dysfunction-
dc.subjecttestosterone blood level-
dc.subjecttype 2 5alpha reductase deficiency-
dc.subjectAdolescent-
dc.subjectAdult-
dc.subjectCase-Control Studies-
dc.subjectChild-
dc.subjectChild, Preschool-
dc.subjectFemale-
dc.subjectGlycoproteins-
dc.subjectHumans-
dc.subjectInfant-
dc.subjectInfant, Newborn-
dc.subjectMale-
dc.subjectOrchiectomy-
dc.subjectTesticular Hormones-
dc.subjectTestosterone 5-alpha-Reductase-
dc.titleDiagnosis of 5α-reductase type 2 deficiency: Contribution of anti-Müllerian hormone evaluationen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniversidade Federal da Bahia (UFBA)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationInterdisciplinary Group for Study on Sex Determination and Differentiation School of Medicine State University of Campinas, Campinas-
dc.description.affiliationMolecular Biology and Genetic Engineering Center School of Medicine State University of Campinas, Campinas-
dc.description.affiliationPhysiology Laboratory Clinical Pathology Department State University of Campinas, Campinas-
dc.description.affiliationPediatrics Department School of Medicine Federal University of Bahia, Salvador-
dc.description.affiliationUnit of Pediatric Endocrinology School of Medicine State University of São Paulo, São Paulo-
dc.description.affiliation, Rua Giuseppe Maximo Scolfaro 371, 13083-100 Campinas, SP-
dc.identifier.doi10.1515/JPEM.2005.18.12.1383-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Pediatric Endocrinology and Metabolism-
dc.identifier.scopus2-s2.0-30944433182-
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