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5 岁男孩患有染色体微重复,表现出破坏性行为、全面发育迟缓与肥胖。

Disruptive Behavior, Global Developmental Delay, and Obesity in a 5-Year-Old Boy with a Chromosome Microduplication.

机构信息

Developmental Behavioral Pediatrics, Department of Pediatrics, University of California San Diego, Rady Children's Hospital, San Diego, CA.

Dysmorphology and Teratology, Department of Pediatrics, University of California San Diego, Rady Children's Hospital, San Diego, CA.

出版信息

J Dev Behav Pediatr. 2018 Jan;39(1):81-84. doi: 10.1097/DBP.0000000000000528.

Abstract

Ryan is a 5-year-old boy who was seen in a Developmental Behavioral Pediatrics clinic for disruptive behavior and developmental delay. His medical history was notable for a tethered spinal cord repaired at age 4 months, alternating exotropia with multiple surgeries, and obesity (body mass index at 99%). Ryan's development was globally delayed. He sat at age 10 months and walked at 24 months. An Autism Diagnostic Observation Schedule-Toddler module (ADOS-T) was completed at age 19 months and demonstrated little-to-no concern for autism spectrum disorder.Ryan's parents described behavioral challenges including hyperactivity, impulsivity, aggression toward him self and others, severe tantrums, a short attention span, and difficulty sleeping. They also endorsed repetitive behaviors including head rocking, walking in circles, and perseverative speech. Expressive language was significantly limited. There was no family history of autism or intellectual disability.Ryan's physical examination was notable for alternating exotropia, hypertelorism, upslanting palpebral fissures, and obesity. His speech was limited to 1-word utterances. Neurological and general examinations were normal.He was referred for repeat psychological testing at age 5 years. The ADOS-2 (Module 2) was consistent with a classification of autism with a high level of autism-related symptoms. A fragile X test was negative, and microarray demonstrated a microduplication in the region of 2p25.3 including the myelin transcription factor 1-like gene.

摘要

瑞安是一个 5 岁的男孩,因行为障碍和发育迟缓在发育行为儿科学诊所就诊。他的病史包括 4 个月大时接受的脊髓栓系松解术、多次斜视手术和肥胖(体重指数为 99%)。瑞安的发育全面延迟,10 个月时会坐,24 个月时会走。19 个月时进行了自闭症诊断观察量表-幼儿模块(ADOS-T)评估,结果显示自闭症谱系障碍的关注度较低。

瑞安的父母描述了他的行为挑战,包括多动、冲动、对自己和他人的攻击性、严重的发脾气、注意力短暂、睡眠困难。他们还报告了重复行为,包括头部晃动、循环行走和坚持说话。表达性语言明显受限。家族中没有自闭症或智力残疾的病史。

瑞安的体检结果显示斜视交替、远视、眼睑裂上斜和肥胖。他的语言仅限于单字表达。神经和一般检查均正常。

他在 5 岁时被转介进行重复心理测试。ADOS-2(模块 2)的评估结果与自闭症分类一致,具有高水平的自闭症相关症状。脆性 X 测试为阴性,微阵列显示 2p25.3 区域存在微重复,包括髓鞘转录因子 1 样基因。

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