Management of scoliosis in a pediatric patient with lysyl hydroxylase-3 deficiency: a case report.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2024-10-13 DOI:10.1186/s13256-024-04822-7
Mirbahador Athari, Ardeshir Tajbakhsh, Ahmadreza Mirbolook, Maryamsadat Beheshtian, Mobin Forghan, Dariush Abtahi
{"title":"Management of scoliosis in a pediatric patient with lysyl hydroxylase-3 deficiency: a case report.","authors":"Mirbahador Athari, Ardeshir Tajbakhsh, Ahmadreza Mirbolook, Maryamsadat Beheshtian, Mobin Forghan, Dariush Abtahi","doi":"10.1186/s13256-024-04822-7","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>A rare case report of lysyl hydroxylases deficiency undergoing scoliosis surgery.</p><p><strong>Case presentation: </strong>An 8-year-old Persian patient with a known case of lysyl hydroxylases deficiency presented with scoliosis. On physical examination, he had course facial hair, elbow flexion contracture, and knee flexion contracture. He had a history of eye surgery, clubfoot, and hearing problems. He underwent scoliosis surgery with growing rod instrumentation.</p><p><strong>Conclusion: </strong>Surgery can be done in these patients with caution, and the surgeon and anesthesiologist should be aware of potential complications during and after surgery.</p>","PeriodicalId":16236,"journal":{"name":"Journal of Medical Case Reports","volume":"18 1","pages":"474"},"PeriodicalIF":0.9000,"publicationDate":"2024-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11471029/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medical Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s13256-024-04822-7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background: A rare case report of lysyl hydroxylases deficiency undergoing scoliosis surgery.

Case presentation: An 8-year-old Persian patient with a known case of lysyl hydroxylases deficiency presented with scoliosis. On physical examination, he had course facial hair, elbow flexion contracture, and knee flexion contracture. He had a history of eye surgery, clubfoot, and hearing problems. He underwent scoliosis surgery with growing rod instrumentation.

Conclusion: Surgery can be done in these patients with caution, and the surgeon and anesthesiologist should be aware of potential complications during and after surgery.

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
对患有赖氨酰羟化酶-3 缺乏症的儿童脊柱侧凸的治疗:病例报告。
背景:一例罕见的赖氨酰羟化酶缺乏症脊柱侧弯手术病例:一例罕见的赖氨酰羟化酶缺乏症患者接受脊柱侧弯手术的病例报告:一名已知患有赖氨酰羟化酶缺乏症的 8 岁波斯病人因脊柱侧弯而就诊。体格检查时,他面部毛发稀疏,肘关节屈曲挛缩,膝关节屈曲挛缩。他有眼科手术史、马蹄内翻足和听力问题。他接受了脊柱侧弯手术,植入了生长棒器械:结论:这些患者可以谨慎进行手术,外科医生和麻醉师应注意术中和术后可能出现的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
期刊最新文献
Late diagnosis of sickle cell disease in adults still a challenge in developing countries: a case report. Presentation of lumbar intramedullary cavernous hemangioma by spindle-shaped hematoma sign on the spinal MRI: a case report. A novel nonsense RPS26 mutation in a patient with Diamond-Blackfan anemia: a case report. Delayed diagnosis of distal myasthenia gravis: a case report. Conservative surgical repair of placenta increta invading into uterine septum: case report.
×
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