ISOLATED VITAMIN-E-DEFICIENCY IN THE ABSENCE OF FAT MALABSORPTION - FAMILIAL AND SPORADIC CASES - CHARACTERIZATION AND INVESTIGATION OF CAUSES

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  • 1 May 1988
    • journal article
    • research article
    • Vol. 111  (5) , 548-559
Abstract
We observed four young adults, including three siblings, with a progressive neurologic disorder that developed over the first two decades. Electrophysiologic studies revealed mildly delayed nerve conduction, decreased amplitudes of sensory action potentials, and sensory delay in the posterior columns. Known causes of similar neurologic disorders were excluded. Although vitamin E deficiency was well documented, intestinal absorption and plasma lipoprotein transport of vitamin E were normal. Incubation studies in vitro failed to identify a plasma factor causing destruction of circulating vitamin E. There was no clinical or laboratory evidence of steatorrhea caused by gastrointestinal, hepatic, or pancreatic disease. Plasma lipoproteins, apolipoprotein B, and adipose tissue fatty acid compositon were normal. Oral vitamin E therapy restored serum levels to normal and caused neurological improvement in two patients. We postulate that an inherited defect in hepatocyte secretion of vitamin E into lipoproteins may account for this disorder, which occurs in sporadic cases as well as in siblings.