Reconsidering Social-Behavioral Phenotypes in Wolf-Hirschhorn Syndrome: Presentation of Two Cases Diagnosed with Autism Spectrum Disorder.

Danielle M Glad, Elisabeth M Vogt, Kelly L Jones, Lauren E Miller
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Abstract

Objective: Comorbidity of autism spectrum disorder (ASD) and Wolf-Hirschhorn syndrome (WHS) is not well understood. Prior research regarding social functioning in WHS is inconsistent and largely focuses on reporting general social difficulties or positive screening results rather than confirmed ASD diagnoses. This case series aims to promote reconsideration of ASD diagnoses in children with WHS and is the only report of ASD symptoms and confirmed diagnoses in WHS based on a comprehensive diagnostic assessment. Two children with WHS completed comprehensive clinical neuropsychological evaluations.

Method: Neurodevelopmental skills (Mullen Scales of Early Learning), adaptive behavior (Adaptive Behavior Assessment System-3rd Edition; Behavior Assessment System for Children-3rd Edition (BASC-3)), emotional and behavioral functioning (BASC-3), and ASD symptomatology (Childhood Autism Rating Scale-2nd Edition; TELE-ASD-PEDS) were assessed.

Results: Both children demonstrated multiple body system involvement consistent with typical medical complexities of WHS. Neuropsychological profiles of each patient revealed unique strengths and weaknesses, though each were consistent with diagnoses of intellectual developmental disorder and ASD.

Conclusions: This case series demonstrates the need to comprehensively assess rather than merely screen ASD symptomatology in children with WHS, taking into account their degree of cognitive impairment. Increased awareness of this co-occurring diagnosis can help promote early identification by diagnosticians and monitoring by other medical providers caring for children with WHS, thereby enabling families to connect to appropriate intervention services.

重新考虑Wolf-Hirschhorn综合征的社会行为表型:两例诊断为自闭症谱系障碍的表现。
目的:自闭症谱系障碍(ASD)与沃尔夫-赫希霍恩综合征(WHS)的合并症尚不清楚。先前关于自闭症谱系障碍患者社会功能的研究并不一致,而且主要集中在报道一般的社会困难或阳性筛查结果,而不是确诊的自闭症谱系障碍诊断。本病例系列旨在促进对WHS患儿ASD诊断的重新考虑,是唯一一份基于综合诊断评估的WHS患儿ASD症状和确诊诊断的报告。2例WHS患儿完成了全面的临床神经心理学评估。方法:神经发育技能(马伦早期学习量表)、适应行为(适应行为评估系统-第三版);儿童行为评估系统-第三版(BASC-3)),情绪和行为功能(BASC-3),以及ASD症状(儿童自闭症评定量表-第二版);TELE-ASD-PEDS)进行评估。结果:两名儿童均表现出多体系统受累,符合WHS的典型医学复杂性。每个病人的神经心理学档案都显示出独特的优势和劣势,尽管每个人都符合智力发育障碍和自闭症谱系障碍的诊断。结论:该病例系列表明,考虑到认知障碍程度,需要全面评估而不仅仅是筛查WHS患儿的ASD症状。提高对这种同时发生的诊断的认识,有助于促进诊断医师的早期识别和照顾WHS儿童的其他医疗提供者的监测,从而使家庭能够获得适当的干预服务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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