ISSN 1301 - 0883 / E-ISSN 1339 - 3886
 
 







 
 
Search





Ethylmalonic encephalopathy associated with respiratory failure [Eastern J Med]
Eastern J Med. 2016; 21(4): 183-186 | DOI: 10.5505/ejm.2016.69885  

Ethylmalonic encephalopathy associated with respiratory failure

Halil Köse1, Mehmet Hamdi Şahan2, Halil İbrahim Aydin3
1Şanlıurfa Pediatric Diseases Hospital, Pediatric Intensive Care Unit, Şanlıurfa, Turkey
2Kızılaslan Medical Center, Department of Radiology, Gaziantep, Turkey
3Turgut Özal University Faculty of Medicine, Department of Pediatric Metabolism Diseases, Ankara, Turkey

Ethylmalonic encephalopathy (EE) is a rarely encountered metabolic disease with autosomal recessive inheritance and is characterized by development retardation, acrocyanosis, petechiae and chronic diarrhea. In the literature, EE has usually presented itself with neurological disorders, developmental retardation, acrocyanosis and skin lesions. We encountered no case in the literature accompanied by respiratory failure. EE should be considered in the patients with severe respiratory failure, exanthematous skin lesion, acidosis, chronic diarrhea, neurological symptoms and pathological signal increment in the basal ganglia on MRI together with the history of sibling death and consanguineous marriage. Herein, a 2.5-year-old boy case, who presented with exanthematous lesions over the body and respiratory failure and had lactic acidemia, increase in serum C4 and C5 acylcarnitine derivatives, excretion of ethylmalonic acid, methyl succinic acid, isovalerylglycine and isobutyrylglycine in the urine, pathological signal increment in the basal ganglia on CT and MRI, and firstly defined homozygote deletion in the ETHE1 gene in genetic analysis. In conclusion, we intended to emphasize consider underlying EE metabolic disease in the cases with frequent lower respiratory tract infection and respiratory failure in the presence of hypotonia and neuromotor developmental retardation.

Keywords: Brain diseases, metabolic, multiple acyl coenzyme a dehydrogenase deficiency, respiratory insufficiency


Halil Köse, Mehmet Hamdi Şahan, Halil İbrahim Aydin. Ethylmalonic encephalopathy associated with respiratory failure. Eastern J Med. 2016; 21(4): 183-186

Corresponding Author: Halil Köse, Türkiye


TOOLS
Full Text PDF
Print
Download citation
RIS
EndNote
BibTex
Medlars
Procite
Reference Manager
Share with email
Share
Send email to author

Similar articles
PubMed
Google Scholar




 
Copyright © 2018 Eastern Journal of Medicine. All Rights Reserved.
Home        |        Contact
LookUs & OnlineMakale