A Case Report of Klippel-Feil Syndrome Presenting as Tetraplegia

نویسندگان

چکیده

Cervical spine assessment is an important step in patients who sustained trauma. Klippel-Feil syndrome (KFS) a complex with abnormal fusion of cervical vertebrae at C2 and C3, which caused by failure the division or normal segmentation early fetal development. This condition leads to characteristic appearance short neck, low hairline, facial asymmetry, limited neck mobility. People congenital defects like KFS are more prone injury. relatively rare disease. Trivial trauma can lead neurologic symptoms such individuals. We present 32-year-old male, alleged history falls from height traumatic injury his head spine. Following event, he was unable move all four limbs. The patient’s noted. Magnetic resonance imaging (MRI) revealed multilevel (C3-C7) single fused highly uncommon. Myelopathy secondary C3-C4 disk protrusion also seen. patient diagnosed managed conservatively. predisposes owing altered biomechanics leading hypermobility adjacent spine, spondylolisthesis, stenosis, thereby increasing likelihood injuries. Screening identification young children essential as counseling for lesser strenuous activity might avoid neurological promote better outcomes future.

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The Klippel-Feil syndrome: a case report.

Short neck and fusion of cervical vertebrae are observed in several genetic conditions and well-defined syndromes. An 8-year-old boy with a short neck, low-set posterior hairline, deafness and limited neck motion was suspected of having such a condition. Clinical and radiographic examination led to the diagnosis of Klippel-Feil syndrome.

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OBJECTIVE To report the clinical presentation and peculiarity of management of Klippel-Feil syndrome (KFS) at the University of Abuja Teaching Hospital, Gwagwalada. BACKGROUND KFS is a rare pathology that has not been previously reported on in Nigeria. METHODS Case review was employed to report this pathology. RESULT This case is a 10 year old boy with KFS presenting with cosmetic blemish...

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Klippel Feil Syndrome: A Rare Case Report

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[A case of Klippel-Feil syndrome].

We would like to present a case of Klippel-Feil Syndrome in which it is associated with multiple cervical vertebra synostosis, short neck, cervical rib, congenital sclerosis, platybasia, spina-bifida and deafness. We are revising the case history of this syndrome.

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ژورنال

عنوان ژورنال: Cureus

سال: 2023

ISSN: ['2168-8184']

DOI: https://doi.org/10.7759/cureus.41241