Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/194031
Type: Artigo de periódico
Title: Female Pseudohermaphroditism Due To Classical 21-hydroxylase Deficiency In A Girl With Turner Syndrome.
Author: Maciel-Guerra, A T
Guerra, G
Marini, S H
Matias Baptista, M T
Marques-de-Faria, A P
Abstract: We 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.
Subject: Adrenal Hyperplasia, Congenital
Disorders Of Sex Development
Female
Humans
Infant
Steroid 21-hydroxylase
Turner Syndrome
Rights: fechado
Identifier DOI: 
Address: http://www.ncbi.nlm.nih.gov/pubmed/9212186
Date Issue: 1997
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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