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Successful prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

โœ Scribed by Stefan A. Wudy; Janos Homoki; Walter M. Teller


Publisher
Springer
Year
1994
Tongue
English
Weight
779 KB
Volume
153
Category
Article
ISSN
0340-6997

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๐Ÿ“œ SIMILAR VOLUMES


Prenatal diagnosis of congenital adrenal
โœ Dumic, M.; Brkljacic, L.; Plavsic, V.; Zunec, R.; Ille, J.; Wilson, R. C.; Kuvac ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 71 KB ๐Ÿ‘ 2 views

We report on the prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase in 20 at-risk pregnancies (16 salt-wasting and 4 simple virilizing families). We have diagnosed 3 affected fetuses (2 males and 1 female), 3 healthy homozygotes (2 males and 1 female), and 14 healthy heterozy

Prenatal diagnosis of congenital adrenal
โœ Phyllis W. Speiser; Perrin C. White; Jacob Dupont; Deguang Zhu; Arlene B. Mercad ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Springer ๐ŸŒ English โš– 593 KB

The feasibility and accuracy of gene-specific molecular genetic diagnosis for congenital adrenal hyperplasia due to 21-hydroxylase deficiency was studied in a group of 24 pregnancies at 25% risk of carrying an affected fetus. Chorionic villus sampling was performed at 9-10 weeks' gestation. Southern