Accepted on 04 Jun 2015
Submitted on 17 May 2015
A 61-year-old female born of full-term normal delivery after a non-consanguineous marriage, reported congenital short neck with abnormal posture, unilateral sensorineural hearing loss, and migraine. She sought consultation at our center for chronic headaches and reported that when she was a teenager she was misdiagnosed with cervical dystonia. Clinical examination showed head tilt, limitation of movement at the cervical level, and low posterior hair implantation (Video 1). Spinal magnetic resonance imaging revealed vertebral fusion between the medulla and C4 as well as partial splitting between C2 and C3.
Klippel–Feil syndrome (KFS) is a rare congenital disorder (1 in 50,000 people), characterized by a defect in the formation or segmentation of the cervical vertebrae with short neck, low posterior hairline, and limited neck movement.1 Extra-skeletal manifestations and spinal abnormalities including posterior fossa cysts or diastematomyelia may occur in KFS.2
In this case, KFS represents an unusual mimicking dystonia or pseudodystonic syndrome where sustained muscle contractions, unusual twisting movements, and/or abnormal postures occur secondary to underlying abnormalities.
1 Funding: None.
2 Financial Disclosures: None.
3 Conflict of Interest: The authors report no conflict of interest.
We thank the patient for her participation.
Brokinkel, B Wiebe, K Hesselmann, V et al. (2013). Surgical treatment in a patient with Klippel-Feil syndrome and anterior cervical meningomyelocele: A case report and review of literature. Eur Spine J 22: S517–S520. http://dx.doi.org/10.1007/s00586-013-2769-6. [PubMed]
Dickerman, RD, Colle, KO and Mittler, MA (2004). Intramedullary inflammatory mass dorsal to the Klippel–Feil deformity: error in development or response to an abnormal motion segment?. Spinal Cord 42: 720–722. http://dx.doi.org/10.1038/sj.sc.3101645. [PubMed]