Literature DB >> 31243752

[Adolescent with a schizophreniform disorder and recurrent 16p11.2 duplication].

L Castelein, J Steyaert, H Peeters, G van Buggenhout.   

Abstract

Genetic factors play an important role in the development of psychotic disorders. With increasing evidence, several rare copy number variants (cnvs) have been identified as risk factors. We describe a patient who had two psychotic episodes during his adolescence. In this patient, a 16p11.2 duplication was detected. This duplication is a recurrent cnv associated with various somatic and psychiatric phenotypes including psychosis and schizophrenia. The potential clinical relevance of this finding is discussed.

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Year:  2019        PMID: 31243752

Source DB:  PubMed          Journal:  Tijdschr Psychiatr        ISSN: 0303-7339


  1 in total

1.  Novel and de novo point and large microdeletion mutation in PRRT2-related epilepsy.

Authors:  Li Yang; Cuiping You; Shiyan Qiu; Xiaofan Yang; Yufen Li; Feng Liu; Dongqing Zhang; Yue Niu; Liyun Xu; Na Xu; Xia Li; Fang Luo; Junli Yang; Baomin Li
Journal:  Brain Behav       Date:  2020-03-31       Impact factor: 2.708

  1 in total

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