| Literature DB >> 9212186 |
A T Maciel-Guerra1, G Guerra, S H Marini, M T Matias Baptista, A P Marques-de-Faria.
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.Entities:
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Year: 1997 PMID： 9212186 DOI： 10.1111/j.1399-0004.1997.tb02487.x
Source DB: PubMed Journal: Clin Genet ISSN： 0009-9163 Impact factor: 4.438