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一名22号染色体微缺失患者患伴有帕金森症的儿童期起病型精神分裂症。

Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22.

作者信息

Krahn L E, Maraganore D M, Michels V V

机构信息

Department of Psychiatry and Psychology, Mayo Clinic Rochester, Minnesota 55905, USA.

出版信息

Mayo Clin Proc. 1998 Oct;73(10):956-9. doi: 10.4065/73.10.956.

Abstract

The deletion of a gene or genes on chromosome 22q11 is responsible for the velocardiofacial syndrome (VCFS), which is associated with cardiac anomalies, short stature, palate abnormalities, learning disabilities, and developmental delay. Herein we describe a 30-year-old man with VCFS in whom a chronic psychotic disorder originated during childhood. A 10% rate of psychotic disorders has been reported in association with this genetic syndrome. In our patient, the clinical manifestation was complicated by extrapyramidal symptoms that predated the onset of psychotic symptoms. To our knowledge, extrapyramidal symptoms have not previously been reported in a patient with VCFS. The diagnosis of VCFS was confirmed with the fluorescence in situ hybridization probe for VCFS. The role of the atypical antipsychotic drug clozapine is discussed with respect to treating this patient who has severe psychotic symptoms coexisting with extrapyramidal symptoms and seizures. In light of the observation that patients with VCFS have an unexpectedly high rate of psychotic disorders, issues concerning the genetics of schizophrenia are intriguing.

摘要

22q11染色体上一个或多个基因的缺失会导致腭心面综合征(VCFS),该综合征与心脏异常、身材矮小、腭部异常、学习障碍和发育迟缓有关。在此我们描述一名30岁患有VCFS的男性,其在童年期出现了一种慢性精神障碍。据报道,这种遗传综合征患者中精神障碍的发生率为10%。在我们的患者中,临床表现因锥体外系症状而复杂化,这些症状早于精神症状出现。据我们所知,此前尚未有关于VCFS患者出现锥体外系症状的报道。通过针对VCFS的荧光原位杂交探针确诊了VCFS。讨论了非典型抗精神病药物氯氮平在治疗该患有严重精神症状且伴有锥体外系症状和癫痫发作患者中的作用。鉴于观察到VCFS患者精神障碍的发生率意外地高,与精神分裂症遗传学相关的问题引人关注。

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