智力残疾伴室管膜下异位的肝炎性精神分裂症1例

S. Yeshaswini, Shahafas Kongath, M. Vidhyavathi
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引用次数: 0

摘要

室管膜下异位(SH),也称为室周结节性异位,被认为是由神经元迁移缺陷引起的,与癫痫发作和智力残疾有关。智力发育迟缓(IDD)是一种智力受损的智力发育停滞或不完全的情况。尽管SH和IDD经常合并发生,但SH合并IDD的精神分裂症病例较少报道。在PubMed、Scopus和Google Scholar上以IDD、SH和精神分裂症为关键词对科学数据库进行彻底搜索,结果有限,这促使我们报告了这例没有任何癫痫病史的SH患者,他们患上了肝原性精神分裂症。这突出了通过MRI扫描检查IDD和精神病患者是否存在SH的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case report of hebephrenic schizophrenia in intellectual disability with subependymal heterotopia
Subependymal heterotopia (SH), also commonly known as periventricular nodular heterotopia, is believed to result from a faulty neuronal migration which is associated with seizure disorders and intellectual disability. Intellectual developmental delay (IDD) is a condition of arrested or incomplete development of mind with the impairment of intelligence. Although SH and IDD co-occur often, cases of schizophrenia in SH with IDD are less commonly reported. A thorough search of scientific databases with keywords of IDD, SH, and schizophrenia on PubMed, Scopus, and Google Scholar combined yielded limited results, prompting us to report this case of SH without any history of seizures who developed hebephrenic Schizophrenia. This highlights the need to check for the presence of SH by MRI scan in individuals with IDD and psychosis.
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