A Novel Distal 22Q11.21 Microduplication in a 43-Year-Old Male Patient with Mild Intellectual Disability, Social Cognitive Dysfunctions, and Anxiety.

IF 2 Q3 CLINICAL NEUROLOGY Clinical Neuropsychiatry Pub Date : 2023-10-01 DOI:10.36131/cnfioritieditore20230504
Jos Egger, Willem Verhoeven, Wim Verbeeck, Margje Sinnema, Alexander Stegmann, Karijn Stuurop, Nicole De Leeuw
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Abstract

Objective: The chromosome region 22q11.2 is highly susceptible to genomic rearrangements. It has become clear that genomic instability extends distally to the commonly deleted/duplicated region (Low Copy Repeats [LCR] A-D) and that a clear difference exists between the phenotypic presentation of patients with rearrangements in the common region versus that in the distal region (LCR D-H), particularly with respect to developmental and somatic issues. Microdeletions in the 22q11.2 distal region are typically associated with congenital heart defects whereas distal 22q11.2 microduplications are infrequently described and present with a smaller duplicated region and a rather unspecified phenotype.

Method: The present paper provides detailed assessments of a middle-aged male with mild intellectual disability, elsewhere diagnosed with autism spectrum disorder. Because of persisting functional complaints, he was referred for second opinion to a specialized outpatient department.

Results: High resolution SNP-based array analysis demonstrated a ~1.5 Mb distal microduplication in chromosome 22 flanked by LCR region 22C and LCR22E encompassing among others the disease gene MAPK1. No remarkable facial dysmorphisms were noticed. Autism spectrum disorder was ruled out and it was concluded that the patient was primarily suffering from mild intellectual disability and social cognitive dysfunctions with anxieties and suspicious social interactions, to be understood as a disorder within the anxiety spectrum.

Conclusions: The pattern of psychological and psychiatric phenomena was discussed against the background of findings on psychopathology in the chromosome 22 region demarcated by LCR breakpoints C and E. It was suggested that alterations in the MAPK1 gene due to either a deletion or a duplication enhance the vulnerability to develop a psychiatric disorder within the anxiety spectrum.

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一名患有轻度智力障碍、社会认知功能障碍和焦虑症的 43 岁男性患者的新型远端 22Q11.21 微重复。
目的:染色体 22q11.2 区域极易发生基因组重排。目前已明确的是,基因组不稳定性向远端延伸至常见的删除/重复区域(低拷贝重复序列 [LCR] A-D),而且常见区域与远端区域(LCR D-H)重排患者的表型表现存在明显差异,尤其是在发育和躯体问题方面。22q11.2 远端区域的微缺失通常与先天性心脏缺陷有关,而 22q11.2 远端微重复则很少见,表现为较小的重复区域和相当不明确的表型:本文对一名患有轻度智力障碍的中年男性进行了详细评估,他在其他地方被诊断为自闭症谱系障碍。由于持续的功能性主诉,他被转诊到一家专科门诊接受第二意见:基于SNP的高分辨率阵列分析表明,22号染色体上有一个约1.5 Mb的远端微重复,两侧是LCR区域22C和LCR22E,其中包括疾病基因MAPK1。没有发现明显的面部畸形。排除了自闭症谱系障碍的可能性,结论是该患者主要患有轻度智力障碍和社会认知功能障碍,伴有焦虑和可疑的社会交往,可以理解为焦虑谱系障碍:以 LCR 断点 C 和 E 所划分的 22 号染色体区域的精神病理学发现为背景,讨论了心理和精神现象的模式。
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来源期刊
Clinical Neuropsychiatry
Clinical Neuropsychiatry CLINICAL NEUROLOGY-
CiteScore
11.10
自引率
1.60%
发文量
0
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