Quick Search
  Home Journal Information Current Issue Past Issues Services Contact Us  
Articles
Wernicke encephalopathy in children and adolescents 
 
Wernicke encephalopathy in children and adolescents
  Matt Lallas, Jay Desai
 [Abstract] [Full Text] [PDF]   Pageviews: 22114 Times
 
Wernicke encephalopathy in children and adolescents
 
Matt Lallas, Jay Desai
California, USA
 
 
Author Affiliations: Division of Neurology, Children's Hospital Los Angeles, California, USA (Lallas M); Keck School of Medicine of University of Southern California, California, USA (Desai J)
 
Corresponding Author: Jay Desai, MD, 4650 Sunset Boulevard # 82, Los Angeles, CA 90027, USA (Tel: 323-361-2471; Fax: 323-361-1109; Email: jdesai@chla.usc.edu)
 
doi: 10.1007/s12519-014-0506-9
 
 
Background: Wernicke encephalopathy is caused by thiamine (vitamin B1) deficiency. It is generally considered to be a disease of adult alcoholics. However, it is known to occur in the pediatric population and in non-alcoholic conditions.
 
Data sources: We searched PubMed with the key words Wernicke, thiamine, pediatric, children and adolescents and selected publications that were deemed appropriate.
 
Results: The global prevalence rates of hunger, poverty and resultant nutrient deprivation have decreased in the 21st century. However, several scenarios which may predispose to Wernicke encephalopathy may be increasingly prevalent in children and adolescents such as malignancies, intensive care unit stays and surgical procedures for the treatment of obesity. Other predisposing conditions include magnesium deficiency and defects in the SLC19A3 gene causing thiamine transporter-2 deficiency. The classic triad consists of encephalopathy, oculomotor dysfunction and gait ataxia but is not seen in a majority of patients. Treatment should be instituted immediately when the diagnosis is suspected clinically without waiting for laboratory confirmation. Common magnetic resonance findings include symmetric T2 hyperintensities in dorsal medial thalamus, mammillary bodies, periaqueductal gray matter, and tectal plate.
 
Conclusions: Wernicke encephalopathy is a medical emergency. Delay in its recognition and treatment may lead to significant morbidity, irreversible neurological damage or even death. This article aims to raise the awareness of this condition among pediatricians.
 
World J Pediatr 2014;10(4):293-298
 
Key words: ataxia;
                   ophthalmoplegia;
                   thiamine;
                   vitamin B1;
                   Wernicke encephalopathy
 
  [Articles Comment]

  title Author The End Revert Time Revert / Count

  Username:
  Comment Title: 
 
   

 

     
 
     
World Journal of Pediatric Surgery

roger vivier bags 美女 美女

Home  |  Journal Information  |  Current Issue  |  Past Issues  |  Journal Information  |  Contact Us
Children's Hospital, Zhejiang University School of Medicine, China
Copyright 2007  www.wjpch.com  All Rights Reserved Designed by eb