Atypical Gilles de la Tourette Syndrome with beta-mannosidase deficiency.

Frédéric Sedel,Karen Friderici,Katherine Nummy,Catherine Caillaud, Allel Chabli,Alexandra Dürr,Catherine Lubetzki,Yves Agid

ARCHIVES OF NEUROLOGY（2006）

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摘要

This case illustrates the phenotypic variability of inborn errors of metabolism in adults and demonstrates the need to screen inborn errors of metabolism in atypical Gilles de la Tourette syndrome.

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