儿童和青少年粘多糖病的功能描述-病例系列

A. M. Fleming, C. T. Ribeiro, D. Horovitz, Luciana Castaneda Ribeiro, Ana Paula Carvalho Corrêa
{"title":"儿童和青少年粘多糖病的功能描述-病例系列","authors":"A. M. Fleming, C. T. Ribeiro, D. Horovitz, Luciana Castaneda Ribeiro, Ana Paula Carvalho Corrêa","doi":"10.1590/2326-4594-jiems-2019-0010","DOIUrl":null,"url":null,"abstract":"Introduction: Rare health conditions as mucopolysaccharidoses (MPS) can directly influence functioning experiences. Mobility restriction, osteoarticular alterations, leads to delayed neuropsychomotor development are some of the negative impacts of MPS. Aims: The purpose of this study is to evaluate the functioning of children with MPS, from the International Classification of Functioning, Disability, and Health (ICF) perspective. Methodology: It is a case series study with a sample of 15 children and adolescents with MPS with a median age of 12 years, followed in a tertiary hospital in Rio de Janeiro, Brazil. Results: The patients were assessed by the model ICF and results were as following: regarding body functions, most categories presented slight impairment. For mobility of joints and gait, the impairment was severe. Activity and participation with most significant limitations were “learning to read/write”, “read/write”, “listening” and “performing multiple tasks.” In self-care, the main limitations were in “drinking”, “taking care of body parts” and “taking care of one’s health.” Also, there were restrictions on “doing household tasks”, “basic economic transactions”, “community living” and “religion and spirituality”. Conclusion: MPS can have a significant impact in different body systems which act as limiting activities that require body mobility.","PeriodicalId":56346,"journal":{"name":"Journal of Inborn Errors of Metabolism and Screening","volume":"135 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Description of Functioning in Children and Adolescents with Mucopolysaccharidosis - Case series\",\"authors\":\"A. M. Fleming, C. T. Ribeiro, D. Horovitz, Luciana Castaneda Ribeiro, Ana Paula Carvalho Corrêa\",\"doi\":\"10.1590/2326-4594-jiems-2019-0010\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Rare health conditions as mucopolysaccharidoses (MPS) can directly influence functioning experiences. Mobility restriction, osteoarticular alterations, leads to delayed neuropsychomotor development are some of the negative impacts of MPS. Aims: The purpose of this study is to evaluate the functioning of children with MPS, from the International Classification of Functioning, Disability, and Health (ICF) perspective. Methodology: It is a case series study with a sample of 15 children and adolescents with MPS with a median age of 12 years, followed in a tertiary hospital in Rio de Janeiro, Brazil. Results: The patients were assessed by the model ICF and results were as following: regarding body functions, most categories presented slight impairment. For mobility of joints and gait, the impairment was severe. Activity and participation with most significant limitations were “learning to read/write”, “read/write”, “listening” and “performing multiple tasks.” In self-care, the main limitations were in “drinking”, “taking care of body parts” and “taking care of one’s health.” Also, there were restrictions on “doing household tasks”, “basic economic transactions”, “community living” and “religion and spirituality”. Conclusion: MPS can have a significant impact in different body systems which act as limiting activities that require body mobility.\",\"PeriodicalId\":56346,\"journal\":{\"name\":\"Journal of Inborn Errors of Metabolism and Screening\",\"volume\":\"135 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Inborn Errors of Metabolism and Screening\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1590/2326-4594-jiems-2019-0010\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inborn Errors of Metabolism and Screening","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1590/2326-4594-jiems-2019-0010","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

简介:罕见的健康状况如粘多糖病(MPS)可以直接影响功能体验。活动受限,骨关节改变,导致神经精神运动发育延迟是MPS的一些负面影响。目的:本研究的目的是从国际功能、残疾和健康分类(ICF)的角度评估MPS儿童的功能。方法:这是一项病例系列研究,样本为15名中位年龄为12岁的MPS儿童和青少年,随访于巴西里约热内卢里约热内卢的一家三级医院。结果:采用模型ICF对患者进行评估,结果如下:在机体功能方面,大部分类别均出现轻微损伤。在关节活动和步态方面,损伤严重。活动和参与限制最大的是“学习读/写”、“读/写”、“听”和“执行多项任务”。在自我保健方面,主要局限在“饮酒”、“照顾身体部位”和“照顾自己的健康”。此外,对“做家务”、“基本经济交易”、“社区生活”和“宗教和精神”也有限制。结论:MPS可以对不同的身体系统产生重大影响,这些系统可以限制需要身体活动的活动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Description of Functioning in Children and Adolescents with Mucopolysaccharidosis - Case series
Introduction: Rare health conditions as mucopolysaccharidoses (MPS) can directly influence functioning experiences. Mobility restriction, osteoarticular alterations, leads to delayed neuropsychomotor development are some of the negative impacts of MPS. Aims: The purpose of this study is to evaluate the functioning of children with MPS, from the International Classification of Functioning, Disability, and Health (ICF) perspective. Methodology: It is a case series study with a sample of 15 children and adolescents with MPS with a median age of 12 years, followed in a tertiary hospital in Rio de Janeiro, Brazil. Results: The patients were assessed by the model ICF and results were as following: regarding body functions, most categories presented slight impairment. For mobility of joints and gait, the impairment was severe. Activity and participation with most significant limitations were “learning to read/write”, “read/write”, “listening” and “performing multiple tasks.” In self-care, the main limitations were in “drinking”, “taking care of body parts” and “taking care of one’s health.” Also, there were restrictions on “doing household tasks”, “basic economic transactions”, “community living” and “religion and spirituality”. Conclusion: MPS can have a significant impact in different body systems which act as limiting activities that require body mobility.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
0.60
自引率
0.00%
发文量
7
审稿时长
12 weeks
期刊介绍: The Journal of Inborn Errors of Metabolism and Screening (JIEMS) is an online peer-reviewed open access journal devoted to publishing clinical and experimental research in inherited metabolic disorders and screening, for health professionals and scientists. Original research articles published in JIEMS range from basic findings that have implications for disease pathogenesis and therapy, passing through diagnosis and screening of metabolic diseases and genetic conditions, and therapy development and outcomes as well. Original articles, reviews on specific topics, brief communications and case reports are welcome. JIEMS aims to become a key resource for geneticists, genetic counselors, biochemists, molecular biologists, reproductive medicine researchers, obstetricians/gynecologists, neonatologists, pediatricians, pathologists and other health professionals interested in inborn errors of metabolism and screening.
期刊最新文献
Clinical Profile Among Brazilian Mucopolysaccharidosis type II Patients: Subgroup Analysis from the Hunter Outcome Survey Familial chylomicronemia syndrome: A comprehensive clinical and genetic approach Characterization of the SRD5A3-CDG Clinical Spectrum Assessing small fiber neuropathy and subtle cardiac involvement in Fabry disease Newborn Screening Program for Cystic Fibrosis in Cuba: Three Years’ Experience
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1