| Literature DB >> 12629249 |
P C Goldenberg1, R D Steiner, L S Merkens, T Dunaway, R A Egan, E A Zimmerman, G Nesbit, B Robinson, N G Kennaway.
Abstract
Leigh syndrome (LS) is a heterogeneous disorder, usually due to a defect in oxidative metabolism. Typically, signs and symptoms commence in infancy or childhood, although rare cases of adult onset have been described. Progressive deterioration is the norm. The authors describe a 22-year-old woman with partial cytochrome c oxidase deficiency who developed fulminant LS following an acute febrile illness and who subsequently showed dramatic clinical and neuroradiologic improvement.Entities:
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Year: 2003 PMID: 12629249 DOI: 10.1212/01.wnl.0000049460.72439.7f
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910