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

• Príomhchruthaitheoirí: Heves Kırmızıbekmez (Údar), Rahime Gül Yesiltepe Mutlu (Údar), Serdar Moralıoğlu (Údar), Ahmet Tellioğlu (Údar), Ayşenur Cerrah Celayir (Údar)
• Formáid: LEABHAR
• Foilsithe / Cruthaithe: Hindawi Limited, 2015-01-01T00:00:00Z.
• Ábhair: article
• Rochtain ar líne: Connect to this object online.

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...