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Urosepsis in infants with vesicoureteral reflux masquerading as the salt-losing type of congenital adrenal hyperplasia

โœ Scribed by Y. N. Vaid; R. L. Lebowitz


Publisher
Springer-Verlag
Year
1989
Tongue
English
Weight
709 KB
Volume
19
Category
Article
ISSN
0301-0449

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Mutations in the 3 -hydroxysteroid dehydrogenase (3 -HSD) type II gene have been reported in a small number of affected females. We report a 46,XX girl born to consanguineous parents from Chile. At birth, she had normal but hyperpigmented female external genitalia. At 60 days she presented salt loss