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[Tourette syndrome and reading disorder in a boy with left parietofrontal tract disruption]
D Martín Fernández-Mayoralas1, A Fernández-Jaén1, J J Gómez Herrera2
1Sección de Neuropediatría, Servicio de Neurología, Hospital Universitario, Pozuelo de Alarcón, Madrid, España.
Abstract:
We present the case of a nine-year-old boy with Tourette syndrome and reading disorder with a history of a severe infectious process in the late neonatal period. Brain MRI showed a left parietal malacotic cavity and diffusion tensor imaging and tractography showed a striking disruption of the white matter bundle that joins the left parietal region with the ipsilateral frontal region with involvement of the left superior longitudinal fasciculus and of the left arcuate fasciculus. Although Tourette syndrome and reading disorder are fundamentally hereditary neuropsychiatric disorders, they can also occur secondary to cerebral alterations like those existing in this boy. The introduction of modern neuroimaging techniques in patients with neuropsychiatric disorders (or the risk of developing them) can be very useful in the diagnosis and prognosis in the future.
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