Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency

M David, MG Forest - The Journal of pediatrics, 1984 - Elsevier
M David, MG Forest
The Journal of pediatrics, 1984Elsevier
In an attempt to prevent in utero virilization of female fetuses with 21-hydroxylase deficiency,
six mothers at risk were treated with either hydrocortisone (n= 1) or dexamethasone (n= 5) in
early pregnancy. Treatment was continued to term in the two pregnancies in which the
diagnosis of an affected female fetus was confirmed. In patient 1 (hydrocortione treatment)
fetal adrenal suppression was only partial but the external genitalia were only slightly
abnormal. In patient 2 (dexamethasone treatment) fetal adrenal suppression was achieved …
In an attempt to prevent in utero virilization of female fetuses with 21-hydroxylase deficiency, six mothers at risk were treated with either hydrocortisone (n=1) or dexamethasone (n=5) in early pregnancy. Treatment was continued to term in the two pregnancies in which the diagnosis of an affected female fetus was confirmed. In patient 1 (hydrocortione treatment) fetal adrenal suppression was only partial but the external genitalia were only slightly abnormal. In patient 2 (dexamethasone treatment) fetal adrenal suppression was achieved and the external genitalia were normal at birth. These encouraging results open a new prospect for treating congenital adrenal hyperplasia in utero.
Elsevier