A Case of ECHS1 Deficiency with Severe Encephalopathy and Status Epilepticus after a Propofol Sedation: Case Report
Conclusion This case report describes the clinical symptoms and the diagnostics of ECHS1 deficiency. It shows the importance of further metabolic and genetic testing of patients with motoric conspicuities and developmental delay. It is important to be cautious with propofol sedation of patients who present an unknown neurological disorder, when metabolic disturbance or especially mitochondriopathy is suspected. [...] Georg Thieme Verlag KG Rüdigerstraße 14, 70469 Stuttgart, GermanyArticle in Thieme eJournals: Table of contents | Abstract | Full text
Source: Neuropediatrics - Category: Neurology Authors: Preusse, Matthias Paraschaki, Georgia Lutz, Soeren Tags: Short Communication Source Type: research
More News: Brain | Diprivan | Genetics | Georgia Health | Lebanon Health | Leigh Syndrome | MRI Scan | Neurology | Propofol