Publication | Open Access
Kearns‐sayre syndrome with reduced plasma and cerebrospinal fluid folate
83
Citations
22
References
1983
Year
Down SyndromeFolate DeficiencyMendelian DisorderCorticobasal DegenerationNeurological DisorderInherited Metabolic DiseasePhysiologyFluid FolatePathologyDegenerative DiseaseCerebrospinal Fluid FolateNeurologyNeuroscienceNeuropathologyMedicineBilateral CalcificationLysosomal Storage DiseaseMovement Disorders
A young woman with Kearns-Sayre syndrome and progressive central nervous system deterioration over 15 years had decreased plasma and cerebrospinal fluid folate levels while receiving phenytoin for a seizure disorder. A muscle biopsy showed a "ragged red fiber" myopathy with reduced muscle carnitine and mitochondrial enzymes. Computed tomographic brain scans showed cerebral white matter hypodensities and bilateral calcification of the basal ganglia. The mechanism for the folate deficiency and altered ratio of plasma to cerebrospinal fluid folate is unknown, but the deficiency may be responsive to replacement therapy.
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