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Type: Artigo de periódico
Title: Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome
Author: MacielGuerra, AT
Guerra, G
Marini, SHVL
Baptista, MTM
MarquesdeFaria, AP
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: congenital adrenal hyperplasia
female pseudohermaphroditism
Turner syndrome
Country: Dinamarca
Editor: Munksgaard Int Publ Ltd
Citation: Clinical Genetics. Munksgaard Int Publ Ltd, v. 51, n. 5, n. 351, n. 353, 1997.
Rights: fechado
Date Issue: 1997
Appears in Collections:Unicamp - Artigos e Outros Documentos

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