Concurrence of Meningomyelocele and Salt-Wasting Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Joint Authors
Kırmızıbekmez, Heves
Yesiltepe Mutlu, Rahime Gül
Moralıoğlu, Serdar
Tellioğlu, Ahmet
Cerrah Celayir, Ayşenur
Source
Issue
Vol. 2015, Issue 2015 (31 Dec. 2015), pp.1-4, 4 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2015-01-19
Country of Publication
Egypt
No. of Pages
4
Main Subjects
Abstract EN
Congenital adrenal hyperplasia (CAH) is a group of inherited defects of cortisol biosynthesis.
A case of classical CAH due to 21-hydroxylase deficiency (21-OHD) with early onset of salt waste and concurrence of meningomyelocele (MMC) was presented here.
The management of salt-wasting crisis which is complicated by a postrenal dysfunction due to neurogenic bladder was described.
Possible reasons of growth retardation in the one-year follow-up period were discussed.
A significant regression of the phallus with proper medical treatment was also mentioned.
American Psychological Association (APA)
Kırmızıbekmez, Heves& Yesiltepe Mutlu, Rahime Gül& Moralıoğlu, Serdar& Tellioğlu, Ahmet& Cerrah Celayir, Ayşenur. 2015. Concurrence of Meningomyelocele and Salt-Wasting Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. Case Reports in Pediatrics،Vol. 2015, no. 2015, pp.1-4.
https://search.emarefa.net/detail/BIM-1059756
Modern Language Association (MLA)
Kırmızıbekmez, Heves…[et al.]. Concurrence of Meningomyelocele and Salt-Wasting Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. Case Reports in Pediatrics No. 2015 (2015), pp.1-4.
https://search.emarefa.net/detail/BIM-1059756
American Medical Association (AMA)
Kırmızıbekmez, Heves& Yesiltepe Mutlu, Rahime Gül& Moralıoğlu, Serdar& Tellioğlu, Ahmet& Cerrah Celayir, Ayşenur. Concurrence of Meningomyelocele and Salt-Wasting Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. Case Reports in Pediatrics. 2015. Vol. 2015, no. 2015, pp.1-4.
https://search.emarefa.net/detail/BIM-1059756
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1059756
