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Inicio Clínica e Investigación en Ginecología y Obstetricia Déficit congénito de 21-α-hidroxilasa. Seudohermafroditismo femenino
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Vol. 28. Núm. 8.
Páginas 340-343 (Enero 2001)
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Vol. 28. Núm. 8.
Páginas 340-343 (Enero 2001)
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Déficit congénito de 21-α-hidroxilasa. Seudohermafroditismo femenino
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I. Narbona, M.A. Barber, I. Eguiluz, L. Alonso, J.V. Hijano, T. Pérez-Reyes, E. Torres, I. Aguilera, I. Cohen, M. Abehsera
Departamento de Obstetricia y Ginecología. Hospital Regional Carlos Haya. Málaga. España
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Resumen

Descripción de los casos de tres hermanas con HSC por déficit de 21-α-hidroxilasa acontecidos en nuestro centro. Revisión de la más reciente bibliografía, y comentarios sobre el diagnóstico precoz y el tratamiento tanto prenatal como neonatal.

Summary

We describe the cases of three sisters with CAH due to 21-hydroxylase deficiency which occurred in our centre. We review the most recent bibliography and comments on early diagnosis and treatment, both prenatal and neonatal

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Bibliografía
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Copyright © 2001. Elsevier España, S.L.. Todos los derechos reservados
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