Open AccessAtypical Gilles de la Tourette Syndrome With β-Mannosidase Deficiency
Author(s) -
Frédéric Sedel,
Karen H. Friderici,
Katherine A. Nummy,
Catherine Caillaud,
A. Chabli,
Alexandra Dürr,
Catherine Lubetzki,
Yves Agid
Publication year - 2006
Publication title -
archives of neurology
Language(s) - Uncategorized
Resource type - Journals
eISSN - 1538-3687
pISSN - 0003-9942
DOI - 10.1001/archneur.63.1.129
Subject(s) - tourette syndrome , inborn error of metabolism , psychology , impulsivity , medicine , pediatrics , psychiatry
beta-Mannosidosis is a rare inborn error of metabolism with various phenotypes, including mental retardation, behavioral problems, hearing loss, and recurrent airway infections in childhood. To our knowledge, there is no published description of Gilles de la Tourette syndrome in association with this enzymatic deficiency.