Autosomal dominant acute necrotising encephalopathy: A case report with possible disease-expression modification by coincidental homocysteinuria

European Journal of Paediatric Neurology

Volumn 15, Issue 2, 2011, Pages 174-176

  Gilson, Clare ^a   McFarland, Robert ^a   Forsyth, Rob ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

Autosomal dominant acute necrotising encephalopathy; Coma; Metabolic disease inherited; Mitochondrial disease

Indexed keywords

CYSTATHIONINE BETA SYNTHASE; PHENYTOIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; CLONIC SEIZURE; COMA; COMORBIDITY; FEMALE; HOMOCYSTINURIA; HUMAN; LEARNING DISORDER; LEIGH DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PRESCHOOL CHILD; PRIORITY JOURNAL; SEIZURE;

ACUTE DISEASE; BRAIN DISEASES, METABOLIC; CHILD, PRESCHOOL; CHROMOSOME DISORDERS; FEMALE; GENES, DOMINANT; GENETIC PREDISPOSITION TO DISEASE; HOMOCYSTINURIA; HUMANS; NECROSIS;

EID: 79952537062     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2010.05.006     Document Type: Article

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