Late prenatal dexamethasone and phenotype variations in 46,XX CAH: Concerns about current protocols and benefits for surgical procedures

Author:

Gorduza Daniela,Tardy-Guidollet Véronique,Robert Elsa,Gay Claire-Lise,Chatelain Pierre,David Michel,Bretones Patricia,Lienhardt-Roussie Anne,Brac de la Perriere Aude,Morel Yves,Mouriquand Pierre

Publisher

Elsevier BV

Subject

Urology,Pediatrics, Perinatology, and Child Health

Reference41 articles.

1. Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency;David;J Pediat,1984

2. Prenatal dexamethasone treatment in pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency – effect on midgestational amniotic fluid steroid levels;Dorr;J Clin Endocrinol Metab,1993

3. Prenatal therapy in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: retrospective follow-up of 253 treated pregnancies in 215 families;Forest;Endocrinologist,1993

4. Prenatal diagnosis and treatment of 21-hydroxylase deficiency;Forest;J Steroid Biochem Mol Biol,1993

5. Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasia;Lajic;J Clin Endocrinol Metab,1998

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