Journal of Pediatric Neurology 2009; 07(03): 317-320
DOI: 10.3233/JPN-2009-0296
Case Report
Georg Thieme Verlag KG Stuttgart – New York

Menkes disease: MRI appearance of a rare neurodegenerative disorder

Janine Rennert
a   Department of Radiology, University of Regensburg, School of Medicine, Regensburg, Germany
,
Regina Doelken
b   Department of Pediatrics, University of Erlangen Medical School, Erlangen, Germany
,
Marc Doelken
c   Department of Neuroradiology, University of Erlangen Medical School, Erlangen, Germany
,
Arnd Doerfler
c   Department of Neuroradiology, University of Erlangen Medical School, Erlangen, Germany
› Author Affiliations

Subject Editor:
Further Information

Publication History

02 July 2008

28 October 2008

Publication Date:
30 July 2015 (online)

Abstract

Leukoencephalopathy and cerebral atrophy occur as prominent radiological features in early onset neurodegenerative disorders of inherited metabolic origin. Menkes disease is a rare X-linked recessive disorder, characterized by neurodevelopmental delay in early infancy, failure to thrive and seizures. While diagnosis of Menkes disease is usually based upon clinical, genetic and laboratory findings, typical radiolological features such as extensive lesions in the white and grey matter are present. Alterations found in more advanced stages are generalized atrophy and vascular changes. We present the case of a 10-month-old boy with Menkes disease, showing extensive abnormal signal of cerebral white matter, followed by generalized cerebral atrophy in magnetic resonance imaging.