Artículos de revistas
Female pseudohermaphroditism due to classical 21-hydroxylase deficiency in a girl with Turner syndrome
Registro en:
Clinical Genetics. Munksgaard Int Publ Ltd, v. 51, n. 5, n. 351, n. 353, 1997.
0009-9163
WOS:A1997XE91800012
Autor
MacielGuerra, AT
Guerra, G
Marini, SHVL
Baptista, MTM
MarquesdeFaria, AP
Institución
Resumen
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. 51 5 351 353