|
|
||||||||
From the Departments of Gynecology and Obstetrics, Physiology, and Pediatrics at the University of Kansas Medical Center and the Ralph Smith Mental Retardation Center, Kansas City, Kansas, and the Department of Obstetrics and Gynecology at the Harvard Medical School, Boston Hospital for Women, Boston, Massachusetts.
Abstract
Fetal adrenal hypoplasia should be considered in pregnant patients with family histories of the condition and/or following observation of drastically reduced maternal estriol excretion. Antepartum diagnosis is important in the clinical management of these infants since deteriorating adrenal function frequently follows an asymptomatic period during the early neonatal life. Antepartum and neonatal diagnostic studies can identify fetal adrenal hypoplasia.
This article has been cited by other articles:
![]() |
N. Weintrob, J. Drouin, S. Vallette-Kasic, E. Taub, D. Marom, Y. Lebenthal, G. Klinger, E. Bron-Harlev, and M. Shohat Low Estriol Levels in the Maternal Triple-Marker Screen as a Predictor of Isolated Adrenocorticotropic Hormone Deficiency Caused by a New Mutation in the TPIT Gene Pediatrics, February 1, 2006; 117(2): e322 - e327. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Vallette-Kasic, T. Brue, A.-M. Pulichino, M. Gueydan, A. Barlier, M. David, M. Nicolino, G. Malpuech, P. Dechelotte, C. Deal, et al. Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by TPIT Gene Mutations J. Clin. Endocrinol. Metab., March 1, 2005; 90(3): 1323 - 1331. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |