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|Type:||Artigo de periódico|
|Title:||Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome|
|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|
|Editor:||Munksgaard Int Publ Ltd|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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