Concurrence of Meningomyelocele and Salt-Wasting Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

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...

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Detalles Bibliográficos
Autores principales: Kırmızıbekmez, Heves, Yesiltepe Mutlu, Rahime Gül, Moralıoğlu, Serdar, Tellioğlu, Ahmet, Cerrah Celayir, Ayşenur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313520/
https://www.ncbi.nlm.nih.gov/pubmed/25685584
http://dx.doi.org/10.1155/2015/196374

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313520/
https://www.ncbi.nlm.nih.gov/pubmed/25685584
http://dx.doi.org/10.1155/2015/196374

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