Review Article
Congenital Adrenal Hyperplasia-Associated Encephalopathy: A Case Report
Faruk Incecik* and Ozlem M Herguner
Divisions of Neurology, Department of Pediatrics Çukurova University, Adana, Turkey
Faruk Incecik, Divisions of Neurology, Department of Pediatrics Çukurova University, Adana, Toros mah. 78186 sok., Yeşilpark Evleri, Kat: 7, no: 13, Adana, Turkey
Received Date: July 05, 2022; Published Date: July 26, 2022
Congenital Adrenal Hyperplasia is a group of autosomal recessive disorders due to deficiencies of enzymes involved in steroidogenesis. Clinical manifestations depend on the degree of cortisol and aldosterone deficiency. The salt-wasting form can present as a medical emergency with severe hyponatremic dehydration, hyperkalemia, polyuria and hyperpigmentation. However, in recent years, patients with CAH presenting with acute encephalopathy or encephalopathic episodes have been reported. We report here clinical and nueroimaging findings of a case with CAH presenting with acute encephalopathy.
Keywords:Congenital adrenal hyperplasia; Acute encephalopathy; Children
-
Faruk Incecik* and Ozlem M Herguner. Congenital Adrenal Hyperplasia-Associated Encephalopathy: A Case Report. Arch Neurol & Neurosci. 12(5): 2022. ANN.MS.ID.000797.
-
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.