Suppr超能文献

儿童期起病的不宁腿综合征

Childhood-onset restless legs syndrome.

作者信息

Kotagal Suresh, Silber Michael H

机构信息

Division of Child and Adolescent Neurology, Mayo Clinic, Rochester, MN, USA.

出版信息

Ann Neurol. 2004 Dec;56(6):803-7. doi: 10.1002/ana.20292.

Abstract

The clinical characteristics of childhood-onset restless legs syndrome are described. Thirty-two of 538 subjects (5.9%) examined in our sleep disorders center received diagnoses of restless legs syndrome. They were classified based on published criteria into probable (n = 9/32 or 28%) and definite (n = 23/32 or 78%) categories. Apart from an earlier age of diagnosis of the probable group, no differences were found between the two categories. Sleep onset or sleep maintenance insomnia was the most common symptoms, being present in 28 of 32 subjects (87.5%). Inattentiveness was seen in 8 of 32 subjects (25%). Serum ferritin levels were measured in 24 of 32 subjects and were below 50 microg/L in 20 of 24 subjects (83%). A family history of restless legs syndrome was present in 23 of 32 (72%) subjects, with mothers almost three times more likely to be affected than fathers (p = 0.02). We conclude that iron deficiency and a strong family history are characteristic of childhood-onset restless legs syndrome.

摘要

描述了儿童期起病的不宁腿综合征的临床特征。在我们睡眠障碍中心接受检查的538名受试者中,有32名(5.9%)被诊断为不宁腿综合征。根据已发表的标准,他们被分为可能(n = 9/32或28%)和确诊(n = 23/32或78%)两类。除了可能组的诊断年龄较早外,两类之间未发现差异。入睡或维持睡眠困难是最常见的症状,32名受试者中有28名(87.5%)出现此症状。32名受试者中有8名(25%)注意力不集中。32名受试者中有24名检测了血清铁蛋白水平,其中24名中的20名(83%)低于50μg/L。32名受试者中有23名(72%)有不宁腿综合征家族史,母亲受影响的可能性几乎是父亲的三倍(p = 0.02)。我们得出结论,缺铁和强烈的家族史是儿童期起病的不宁腿综合征的特征。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验