PEDIATRICS Vol. 29 No. 5 May 1962, pp. 828-830
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FEMALE PSEUDOHEMAPHRODITISM WITH DELIVERY OF A NORMAL CHILD

Joseph Avin M.D.1

1 Department of Pediatrics, Maimonides Hospital, Brooklyn, New York

A typical case of congenital adrenocortical hyperplasia with a persistent urogenital sinus has been followed for 9 years from the initiation of steroid therapy at 12 years, through surgical correction of the genital anomalies, a ruptured tubal pregnancy, and finally to the delivery of a normal female infant. The literature is briefly reviewed.




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J. C. Lo, V. M. Schwitzgebel, J. B. Tyrrell, P. A. Fitzgerald, S. L. Kaplan, F. A. Conte, and M. M. Grumbach
Normal Female Infants Born of Mothers with Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
J. Clin. Endocrinol. Metab., March 1, 1999; 84(3): 930 - 936.
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