Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/196545
Type: Artigo de periódico
Title: Diagnosis Of 5alpha-reductase Type 2 Deficiency: Contribution Of Anti-müllerian Hormone Evaluation.
Author: Stuchi-Perez, Eliana G
Hackel, Christine
Oliveira, Luiz Eduardo C
Ferraz, Lucio F C
Oliveira, Laurione C
Nunes-Silva, Daniela
Toralles, Maria Betania
Steinmetz, Leandra
Damiani, Durval
Maciel-Guerra, Andrea T
Guerra-Junior, Gil
Abstract: To evaluate anti-Müllerian hormone (AMH) levels in patients with clinical and molecular diagnosis of 5alpha-reductase 2 deficiency. 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. 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. Prepubertal patients with 5alpha-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.
Subject: 3-oxo-5-alpha-steroid 4-dehydrogenase
Adolescent
Adult
Anti-mullerian Hormone
Case-control Studies
Child
Child, Preschool
Dihydrotestosterone
Female
Glycoproteins
Humans
Infant
Infant, Newborn
Male
Orchiectomy
Testicular Hormones
Testosterone
Rights: fechado
Identifier DOI: 
Address: http://www.ncbi.nlm.nih.gov/pubmed/16459464
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

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