[Sleep disorders in early childhood with chronic somatic conditions and atypical development - with particular reference to Down syndrome].

IF 0.9 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Orvosi hetilap Pub Date : 2024-09-08 DOI:10.1556/650.2024.33041
Noémi Napravszky, Ágnes Gulácsi, Mária Alkonyi, Ildikó Danis
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Abstract

Literature and parental reports suggest that young children with chronic illness or disability, particularly those diagnosed with neurodevelopmental disorders, have a significantly higher prevalence of sleep problems than typically developing children of similar age. In the majority of cases, symptoms have a multifactorial etiology, with the child’s somatic condition, associated neurological and psychiatric disorders, as well as relationship characteristics and environmental circumstances, influencing their presentation. In groups of children with chronic illness, atypical developmental trajectories, specific neurological functioning and behavioral phenotypes, sleep disorders are underdiagnosed because it is difficult to separate the child’s illness from the characteristics and consequences of sleep symptoms in the complex symptom picture. For families of children with chronic illnesses or disabilities, the presence of sleep disorders can further complicate adjustment to more challenging life situations and have a significant impact on the well-being and quality of life of the family members. Children with Down syndrome face the challenges of the special needs groups of children that are the focus of our study, where syndrome-specific features, chronic somatic conditions, and structural and functional changes in the nervous system contribute in complex ways to the increased prevalence of sleep-related problems. In addition to early identification of sleep problems, prevention and intervention initiatives in practice can prevent, treat and alleviate a range of short- and long-term negative developmental and behavioral consequences, and contribute to improving the relationship characteristics and quality of life of affected children and their families. Orv Hetil. 2024; 165(36): 1411–1422.

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[幼儿期睡眠障碍与慢性躯体疾病和非典型发育有关--特别是与唐氏综合征有关]。
文献和家长报告表明,患有慢性疾病或残疾的幼儿,特别是那些被诊断为神经发育障碍的幼儿,比同龄正常发育的儿童有明显更高的睡眠问题患病率。在大多数情况下,症状具有多因素的病因,儿童的躯体状况、相关的神经和精神疾病,以及关系特征和环境情况影响了症状的表现。在患有慢性疾病、非典型发育轨迹、特定神经功能和行为表型的儿童群体中,睡眠障碍的诊断不足,因为在复杂的症状图景中,很难将儿童的疾病与睡眠症状的特征和后果区分开来。对于有慢性疾病或残疾儿童的家庭来说,睡眠障碍的存在会使适应更具挑战性的生活环境变得更加复杂,并对家庭成员的福祉和生活质量产生重大影响。唐氏综合症儿童面临着特殊需要儿童群体的挑战,这是我们研究的重点,其中综合征特异性特征,慢性躯体疾病以及神经系统的结构和功能变化以复杂的方式促进了睡眠相关问题的患病率增加。除了早期识别睡眠问题,预防和干预措施在实践中可以预防、治疗和减轻一系列短期和长期的负面发展和行为后果,并有助于改善受影响儿童及其家庭的关系特征和生活质量。奥夫·海泰尔。2024;165(36): 1411 - 1422。
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来源期刊
Orvosi hetilap
Orvosi hetilap MEDICINE, GENERAL & INTERNAL-
CiteScore
1.20
自引率
50.00%
发文量
274
期刊介绍: The journal publishes original and review papers in the fields of experimental and clinical medicine. It covers epidemiology, diagnostics, therapy and the prevention of human diseases as well as papers of medical history. Orvosi Hetilap is the oldest, still in-print, Hungarian publication and also the one-and-only weekly published scientific journal in Hungary. The strategy of the journal is based on the Curatorium of the Lajos Markusovszky Foundation and on the National and International Editorial Board. The 150 year-old journal is part of the Hungarian Cultural Heritage.
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