{"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.