A Rare Presentation of Hyperphagia and Parasomnias Associated With Chromosome 4q Deletion: A Case Report.

Q4 Medicine
Case Reports in Psychiatry Pub Date : 2025-04-01 eCollection Date: 2025-01-01 DOI:10.1155/crps/5061704
Sarah L Vaithilingam, Sheldon R Garrison, Aman Mahajan, Julia F Kranz, John T Diener
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引用次数: 0

Abstract

Background: Chromosome 4q deletion is a rare genetic disorder affecting an estimated 1 out of 100,000 people. It is characterized by microdeletions of the long arm of chromosome 4 with variable clinical presentations including heart defects, craniofacial and skeletal abnormalities, short stature, and developmental delays. While behavioral and psychiatric symptoms have been reported in a small number of patients with chromosome 4q deletions, none of these reports have described the hyperphagia or parasomnia symptoms that are presented in the current case. Case Presentation: A 7-year-old boy presented with a microdeletion of the long arm of chromosome 4 that resulted in psychiatric symptoms and neurodevelopmental delays. Notable manifestations included hyperphagia and parasomnias, in addition to aggression, functional encopresis, and speech delays. The boy's initial treatment was markedly delayed due to limited genetic testing at the age of 1 year, which led to a misdiagnosis of childhood aggression. This limited the care team involvement for neurologic evaluation and appropriate school interventions that would have otherwise been indicated. At inpatient admission, a multidisciplinary approach to diagnosis and treatment was adopted, encompassing pharmacological and behavioral interventions. The patient's attention-deficit/hyperactivity disorder (ADHD) was treated, and his individualized education plan included a functional behavioral assessment, as well as occupational therapy and speech and language services. Following a 4-day inpatient stay, the patient demonstrated a significant decrease in aggressive behaviors. Conclusion: Chromosome 4q deletion-related behaviors parallel those of children with autism spectrum disorder (ASD), and treatment is primarily focused on behavioral interventions. To successfully manage the psychiatric features of this complex condition, the involvement of a multidisciplinary team is recommended.

罕见的与4q染色体缺失相关的贪食和异食症1例报告。
背景:染色体4q缺失是一种罕见的遗传疾病,估计每10万人中就有1人患有这种疾病。其特征是4号染色体长臂微缺失,临床表现多样,包括心脏缺陷、颅面和骨骼异常、身材矮小和发育迟缓。虽然在少数4q染色体缺失的患者中有行为和精神症状的报道,但这些报道都没有描述本病例中出现的嗜食或睡眠异常症状。病例介绍:一名7岁男孩表现为4号染色体长臂微缺失,导致精神症状和神经发育迟缓。显著的表现包括嗜食和睡眠异常,此外还有攻击性、功能性记忆缺失和语言迟缓。由于1岁时有限的基因检测,该男孩的初始治疗明显延迟,导致儿童攻击的误诊。这限制了护理团队参与神经系统评估和适当的学校干预,否则会被指示。在住院时,采用多学科方法进行诊断和治疗,包括药理学和行为干预。患者的注意力缺陷/多动障碍(ADHD)得到了治疗,他的个性化教育计划包括功能行为评估,以及职业治疗和语言服务。住院4天后,患者的攻击行为显著减少。结论:染色体4q缺失相关行为与自闭症谱系障碍(ASD)儿童相似,治疗主要集中在行为干预上。为了成功地管理这种复杂疾病的精神特征,建议多学科团队的参与。
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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来源期刊
Case Reports in Psychiatry
Case Reports in Psychiatry Medicine-Psychiatry and Mental Health
CiteScore
1.00
自引率
0.00%
发文量
49
审稿时长
12 weeks
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