Publication:
Multiple major and minor anomalies associated with Klippel-Feil syndrome: A case report

dc.contributor.authorStupar, Nada Vujasinovic (36549315900)
dc.contributor.authorPavlov-Dolijanovic, Slavica (8452470400)
dc.contributor.authorHatib, Nur (57225255531)
dc.contributor.authorBanko, Bojan (35809871900)
dc.contributor.authorDjukic, Milan (23988377500)
dc.contributor.authorJakoba, Natasa Nikolic (55427357200)
dc.date.accessioned2025-06-12T19:07:54Z
dc.date.available2025-06-12T19:07:54Z
dc.date.issued2016
dc.description.abstractKlippel-Feil syndrome is defined as congenital fusion of two or more cervical vertebrae. In this article, we report a 55-year-old male patient with one-year history of neck pain, headaches, and one episode of syncope after a severe trauma. X-rays and magnetic resonance imaging of cervical spine revealed fused vertebral bodies of C2-C5. The major anomalies associated with Klippel-Feil syndrome (small stature, thoracic kyphoscoliosis, lumbar scoliosis, restricted opening mouth, and bilateral sensorineural hearing loss) as well as multiple minor anomalies (mild face asymmetry, high arched palate, rhinoscoliosis, high nasal bridge, inclined septi nasi, and thin upper lip) were detected. This is a rare case describing the anomalies of the nose in Klippel-Feil syndrome patients. Our patient had no central cord impairment following a severe trauma. ©2016 Turkish League Against Rheumatism. All rights reserved.
dc.identifier.urihttps://doi.org/10.5606/ArchRheumatol.2016.5714
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84961626114&doi=10.5606%2fArchRheumatol.2016.5714&partnerID=40&md5=f85a5409681f675f3b0d0717261d07f7
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/7992
dc.subjectAnomalies
dc.subjectKlippel-Feil syndrome
dc.subjectNeurological symptoms
dc.subjectTrauma
dc.titleMultiple major and minor anomalies associated with Klippel-Feil syndrome: A case report
dspace.entity.typePublication

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