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1.
Clin Neuropharmacol ; 30(2): 114-21, 2007.
Article in English | MEDLINE | ID: mdl-17414944

ABSTRACT

OBJECTIVES: Long-term studies show that 47% to 63% of schizophrenic patients treated with clozapine fail to respond after 12 years of treatment. Such high rates of resistance justify the growing interest in therapeutic strategies based on enhancing the effect of clozapine with other antipsychotics. The combination of clozapine and risperidone in the treatment of partial responders to clozapine has been one of those receiving most interest from research. METHODS AND RESULTS: The present work reports the case of a 26-year-old man, diagnosed with schizophrenia who, after treatment with clozapine at appropriate doses over 12 weeks without observable response, showed a marked and sustained improvement after the addition of risperidone to the clozapine treatment. We also present a detailed review of publications related to the therapeutic combination of clozapine and risperidone in clozapine-resistant schizophrenia. CONCLUSIONS: Despite the contradictory nature of the published data, our results are in support of other work reporting that treatment with a combination of clozapine and risperidone, apart from being well tolerated, may constitute an effective alternative in this type of patient. Nevertheless, there is a need for further, controlled studies, with larger samples, with a view to drawing definitive conclusions and making specific recommendations.


Subject(s)
Antipsychotic Agents/therapeutic use , Clozapine/therapeutic use , Risperidone/therapeutic use , Schizophrenia/drug therapy , Adult , Drug Resistance , Drug Therapy, Combination , Humans , Longitudinal Studies , Male , Psychiatric Status Rating Scales , Review Literature as Topic
2.
Am J Med Genet A ; 140(24): 2807-11, 2006 Dec 15.
Article in English | MEDLINE | ID: mdl-17036352

ABSTRACT

We report on two new patients, the propositus and his maternal uncle, with Lujan-Fryns syndrome (LFS). One presented with mild mental retardation and both patient had Marfanoid habitus and similar craniofacial anomalies (they had a long and narrow face, small mandible, high-arched palate, and hypernasal voice) as previously reported by Lujan et al. in 1984 and Fryns and Buttiens in 1987. One of our patients had agenesis of the corpus callosum as described by Lujan. The second patient had an ascending aortic aneurysm like the patient described by Wittine et al. 1999. Both patients showed similar behavior and psychiatric disorders. In addition, we reviewed the literature for the presence of psychopathology in LFS. After studying the 32 published cases and the 2 described in this article, we found that more than 90% of the patients present with some type of psychopathology, the most frequent being an autistic-like disorder. In our opinion, the agenesis of the corpus callosum (complete or partial) and ascending aorta aneurysm are manifestations of LFS, and thus brain MRI and echocardiogram should be part of the routine evaluation. Additionally, the high prevalence of psychopathological alterations in these patients suggests the need for psychiatric evaluation at the time of diagnosis.


Subject(s)
Marfan Syndrome/psychology , Mental Retardation, X-Linked/psychology , Adult , Agenesis of Corpus Callosum , Craniofacial Abnormalities/complications , Craniofacial Abnormalities/genetics , Craniofacial Abnormalities/psychology , Humans , Male , Marfan Syndrome/complications , Marfan Syndrome/genetics , Mental Retardation, X-Linked/complications , Mental Retardation, X-Linked/genetics , Phenotype , Psychopathology , Syndrome
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