利培酮治疗非癫痫发作障碍和染色体15q缺失综合征

IF 1.3 Q4 NEUROSCIENCES

Progress in Neurology and Psychiatry Pub Date : 2021-10-01 DOI:10.1002/pnp.725

A. Javaid, David Kent, Joanne Bone, D. Michael

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引用次数: 0

摘要

染色体15q11.2微缺失是一种新出现的综合征，在Prader‐Willi综合征和Angelman综合征患者中发现，但也在孤立状态下发现。在这里，作者介绍了一名19岁女性的病例，她患有染色体15q11.2微缺失，并成功地接受了利培酮治疗，制定了一项量身定制的积极行为支持计划，并对工作人员进行了非癫痫发作障碍方面的培训。

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Risperidone in non‐epileptic attack disorder and chromosome 15q deletion syndrome

Chromosome 15q11.2 microdeletion is an emerging syndrome identified in individuals with Prader‐Willi syndrome and Angelman syndrome but also found in isolation. Here, the authors present a case of a 19‐year‐old woman with chromosome 15q11.2 microdeletion and her successful treatment with risperidone, a tailored positive behaviour support plan and with staff training around non‐epileptic attack disorder.

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来源期刊

Progress in Neurology and Psychiatry NEUROSCIENCES-

CiteScore

1.70

自引率

8.30%

发文量

期刊介绍： Progress in Neurology and Psychiatry is published nine times a year, and is a journal for specialists in secondary care, GPs with an interest in neurology and psychiatry, community psychiatric nurses and other specialist healthcare professionals. Articles cover management, news updates and opinion in all areas of neurology and psychiatry.