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Case Reports
. 1989 May;39(5):741-2.
doi: 10.1212/wnl.39.5.741.

Late onset of distinct neurologic syndromes in galactosemic siblings

J H Friedman  1 , H L Levy, R M Boustany
Affiliations
Case Reports

Late onset of distinct neurologic syndromes in galactosemic siblings

J H Friedman et al. Neurology. 1989 May.

Abstract

We discuss siblings with galactose-1-phosphate uridyl transferase deficiency who developed neurologic complications after the age of 30. One has partial complex seizures and the other has generalized seizures, progressive ataxia, and apraxia. As more galactosemic children survive into adulthood, more neurologic complications may become more prevalent.

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