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Lateralized effect of pallidal stimulation on self-mutilation in Lesch-Nyhan disease.
Abel, Taylor J; Dalm, Brian D; Grossbach, Andrew J; Jackson, Adam W; Thomsen, Teri; Greenlee, Jeremy D W.
Afiliação
  • Abel TJ; Departments of Neurosurgery and.
J Neurosurg Pediatr ; 14(6): 594-7, 2014 Dec.
Article em En | MEDLINE | ID: mdl-25303157
Lesch-Nyhan disease (LND) is an X-linked hereditary disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase. This syndrome is characterized by hyperuricemia, self-mutilation, cognitive impairment, and movement disorders such as spasticity and dystonia. The authors describe the case of a 15-year-old boy who underwent bilateral placement of globus pallidus internus (GPi) deep brain stimulation (DBS) electrodes for the treatment of generalized dystonia. His self-mutilating behavior gradually disappeared several weeks after the start of GPi stimulation. The dystonia and self-mutilating behavior returned on the left side only after a right lead fracture. This case is the first reported instance of LND treated with DBS in which the stimulation was interrupted and the self-mutilation returned in a lateralized fashion. The findings indicate that the neurobehavioral aspect of LND is lateralized and that contralateral GPi stimulation is responsible for lateralized improvement in self-injurious behavior.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Comportamento Autodestrutivo / Estimulação Encefálica Profunda / Distonia / Globo Pálido / Lateralidade Funcional / Síndrome de Lesch-Nyhan Limite: Adolescent / Humans / Male Idioma: En Revista: J Neurosurg Pediatr Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Comportamento Autodestrutivo / Estimulação Encefálica Profunda / Distonia / Globo Pálido / Lateralidade Funcional / Síndrome de Lesch-Nyhan Limite: Adolescent / Humans / Male Idioma: En Revista: J Neurosurg Pediatr Ano de publicação: 2014 Tipo de documento: Article