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洛氏眼脑肾综合征中离散行为表型的证据。

Evidence for a discrete behavioral phenotype in the oculocerebrorenal syndrome of Lowe.

作者信息

Kenworthy L, Charnas L

机构信息

Human Genetics Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Am J Med Genet. 1995 Nov 20;59(3):283-90. doi: 10.1002/ajmg.1320590304.

Abstract

The oculocerebrorenal syndrome of Lowe (OCRL) is an X-linked disorder characterized by congenital cataracts, cognitive impairment, and renal tubular dysfunction. Although there is a wide range of intellectual function in affected individuals, it is often compromised by a high prevalence of maladaptive behaviors, including tantrums, stubborness, and stereotypy. Whether these behaviors simply reflect the multiple disabilities found in some developmentally impaired individuals with or without OCRL, or a specific genetically-determined behavioral phenotype of OCRL, is unknown. Controls were matched for sex, age, visual impairment, and adaptive functioning and compared with OCRL patients on three standardized measures of adaptive/maladaptive behaviors. Forty-three matched pairs of OCRL and control subjects were identified. Both groups were similar in communication, daily living, socialization, and motor skills, in socioeconomic status, and in measures of parental stress. Individuals with OCRL displayed significantly more severe maladaptive behaviors than control boys, as measured by the Vineland Adaptive Behavior Scales (VABS), with 41% of the difference between the two groups attributable to the diagnosis of OCRL. Twelve maladaptive behaviors measured on the VABS appeared more frequently in OCRL than in controls. Five of these 12 behaviors, i.e., temper tantrums, irritability, complex repetitive behaviors (stereotypy)/mannerisms, obsessions/unusual preoccupations, and negativism, were identified by discriminant function analysis to significantly distinguish between controls and OCRL individuals. The diagnosis of OCRL is associated with a behavioral phenotype consisting of temper tantrums, stereotypy, stubborness, and obsessions/unusual preoccupations. This phenotype cannot be attributed solely to the visual, motor, and intellectual disabilities characteristic of OCRL, and may represent a specific effect of the OCRL gene on the central nervous system.

摘要

洛氏眼脑肾综合征(OCRL)是一种X连锁疾病,其特征为先天性白内障、认知障碍和肾小管功能障碍。尽管受影响个体的智力功能范围广泛,但往往因适应不良行为的高发生率而受到损害,这些行为包括发脾气、固执和刻板行为。这些行为是仅仅反映了一些有或没有OCRL的发育障碍个体中发现的多种残疾,还是OCRL的一种特定基因决定的行为表型,目前尚不清楚。对照组在性别、年龄、视力障碍和适应性功能方面进行了匹配,并与OCRL患者在三种适应性/适应不良行为的标准化测量指标上进行了比较。确定了43对匹配的OCRL和对照受试者。两组在沟通、日常生活、社交和运动技能、社会经济地位以及父母压力测量方面相似。通过文兰适应性行为量表(VABS)测量,OCRL个体表现出比对照男孩更严重的适应不良行为,两组之间41%的差异可归因于OCRL的诊断。在VABS上测量的12种适应不良行为在OCRL中比在对照组中更频繁出现。通过判别函数分析确定,这12种行为中的5种,即发脾气、易怒、复杂重复行为(刻板行为)/习惯动作、强迫观念/异常关注和消极态度,能够显著区分对照组和OCRL个体。OCRL的诊断与一种行为表型相关,该表型包括发脾气、刻板行为、固执和强迫观念/异常关注。这种表型不能仅仅归因于OCRL特有的视力、运动和智力残疾,可能代表了OCRL基因对中枢神经系统的特定影响。

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