Klippel-Feil Syndrome: A Rare Case Report.

Case Reports in Radiology Pub Date : 2026-05-21 eCollection Date: 2026-01-01 DOI:10.1155/crra/7334537
Mustafa Al Jaafar, Alyaa Nooruldeen Shawqi Aljafr
{"title":"Klippel-Feil Syndrome: A Rare Case Report.","authors":"Mustafa Al Jaafar, Alyaa Nooruldeen Shawqi Aljafr","doi":"10.1155/crra/7334537","DOIUrl":null,"url":null,"abstract":"<p><p>Klippel-Feil syndrome (KFS) is a rare, complex syndrome characterized by abnormal fusion of cervical vertebrae. This case highlights the effectiveness of conservative management in KFS patients without neurological deficits. We reported the case of an 18-year-old Iraqi male presenting a short neck, low back hairline, winged right scapula, and scoliosis after physical examination and deformities of cervical spine fusion, kyphoscoliosis and Sprengel's deformity after imaging tests. Clinical and radiological diagnosis shows KFS. After conservative treatment-including a corrective collar, cervical traction (5 kg), and targeted physiotherapy for 12 months-significant reduction in neck pain and an increase in cervical range of motion were recognized. This case emphasizes the efficiency of conservative management in KFS patients classified as Samartzis Type II with no neurological disabilities.</p>","PeriodicalId":30326,"journal":{"name":"Case Reports in Radiology","volume":"2026 ","pages":"7334537"},"PeriodicalIF":0.0000,"publicationDate":"2026-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13191780/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/crra/7334537","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Klippel-Feil syndrome (KFS) is a rare, complex syndrome characterized by abnormal fusion of cervical vertebrae. This case highlights the effectiveness of conservative management in KFS patients without neurological deficits. We reported the case of an 18-year-old Iraqi male presenting a short neck, low back hairline, winged right scapula, and scoliosis after physical examination and deformities of cervical spine fusion, kyphoscoliosis and Sprengel's deformity after imaging tests. Clinical and radiological diagnosis shows KFS. After conservative treatment-including a corrective collar, cervical traction (5 kg), and targeted physiotherapy for 12 months-significant reduction in neck pain and an increase in cervical range of motion were recognized. This case emphasizes the efficiency of conservative management in KFS patients classified as Samartzis Type II with no neurological disabilities.

Klippel-Feil综合征:罕见病例报告。
klipppel - feil综合征(KFS)是一种罕见的复杂综合征,其特征是颈椎融合异常。本病例强调了保守治疗在无神经功能缺损的KFS患者中的有效性。我们报告了一名18岁的伊拉克男性病例,体格检查后表现为颈部短,背部发际线低,右肩胛骨呈翼状,脊柱侧凸,影像学检查后表现为颈椎融合畸形,后凸性脊柱侧凸和Sprengel畸形。临床及影像学诊断为KFS。经过保守治疗,包括矫正项圈、颈椎牵引(5公斤)和有针对性的物理治疗12个月后,颈部疼痛明显减轻,颈椎活动范围增加。本病例强调对归类为Samartzis II型且无神经功能障碍的KFS患者进行保守治疗的有效性。
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 求助全文
来源期刊
自引率
0.00%
发文量
6
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书