| Literature DB >> 19428206 |
Augusto Pasini1, Elisa D'Agati, Livia Casarelli, Paolo Curatolo.
Abstract
We describe a 18-year-old female with 22q13.3 deletion syndrome characterized by an alteration of SHANK3/PROSAP2 and severe mental retardation, intense psychomotor agitation and aggressive behaviour. When the patient was given risperidone, different therapeutic results were observed: at a 6 mg dose, risperidone had no therapeutic effect and the patient's behavioural problems increased; at a low dose (1mg), risperidone treatment resulted in rapid improvement of mood and behaviour. Recent findings suggest that risperidone exerts dose-dependent effects on Glu receptors in developing rats. An altered preset of the glutamate receptors, due to the presence of a haploinsufficiency of SHANK3/PROSAP2, could explain the different results of risperidone therapy observed in our patient with 22q13.3 deletion syndrome. Copyright 2009 Elsevier B.V. All rights reserved.Entities:
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Year: 2009 PMID: 19428206 DOI: 10.1016/j.braindev.2009.04.005
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961