Palmour R M, Miller S, Fielding A, Vekemans M, Ervin F R
Department of Psychiatry, McGill University, Montreal, Quebec.
J Psychiatry Neurosci. 1994 Jul;19(4):270-7.
A structural abnormality of chromosome 4 [inv 4 (p15.2; q21.3)] is reported in a male presenting with DSM-III-R schizophrenia, undifferentiated type (295.94) and in his mother, who displayed symptoms associated with schizotypal personality disorder (DSM-III-R 301.22). The proband had a performance IQ of 91, poor motor coordination, stature in the lowest quartile and an impaired sense of time. There were no diagnostic physical or neurological abnormalities. Mild ventricular enlargement and prominent sulci were found on computed tomography. Both he and his chromosomally normal father had strabismus which required surgical correction. This case joins the long list of chromosomal abnormalities previously reported to confer an increased risk of mental illness and emphasizes the importance of a sophisticated differential diagnosis in evaluating patients who present with symptoms of schizophrenia. The implications for recent initiatives which attempt to localize genes conferring susceptibility to schizophrenia and other major mental illnesses are discussed.
据报道,一名患有DSM-III-R精神分裂症(未分化型,编码295.94)的男性及其母亲存在4号染色体结构异常[inv 4 (p15.2; q21.3)],其母亲表现出与分裂型人格障碍相关的症状(DSM-III-R编码301.22)。先证者的操作智商为91,运动协调性差,身高处于最低四分位数,时间感知受损。没有诊断出身体或神经方面的异常。计算机断层扫描发现轻度脑室扩大和脑沟增宽。他和染色体正常的父亲都患有斜视,需要手术矫正。该病例加入了先前报道的众多染色体异常病例之列,这些异常会增加患精神疾病的风险,并强调了在评估出现精神分裂症症状的患者时进行精细鉴别诊断的重要性。本文还讨论了近期试图定位导致精神分裂症和其他主要精神疾病易感性基因的研究计划的意义。