Pediatric Neurology Briefs (Dec 1993)

Vitamin E Deficiency Familial Ataxic Syndrome

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-7-12-4
Journal volume & issue
Vol. 7, no. 12
pp. 91 – 92

Abstract

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A total of 8 members of two consanguineous Tunisian families affected with Friedreich’s ataxia (FA) phenotype not linked to chromosome 9 were found to have very low levels of serum vitamin E (0.5 mcg/ml cf 8 mcg/ml in controls) in a study at the Institut National de Neurologie, Tunis, and at Centers in Cyprus and France.

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