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Neurology ; 60(5): 865-8, 2003 Mar 11.
Article in English | MEDLINE | ID: mdl-12629249

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.


Subject(s)
Cytochrome-c Oxidase Deficiency/drug therapy , Leigh Disease/drug therapy , Leigh Disease/enzymology , Adult , Ascorbic Acid/administration & dosage , Brain/pathology , Drug Therapy, Combination , Female , Humans , Leigh Disease/diagnosis , Magnetic Resonance Imaging , Remission Induction , Riboflavin/administration & dosage , Thiamine/administration & dosage , Ubiquinone/administration & dosage
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