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Related Experiment Videos

The Klippel-Feil syndrome: a case report.

Manuel O Lagravère1, María I Barriga, Carla Valdizán

  • 1Faculty of Medicine and Dentistry, Dentistry/Pharmacy Centre, University of Alberta, Edmonton, Alberta, Canada. mlagravere@ualberta.ca

Journal (Canadian Dental Association)
|November 9, 2004
PubMed
Summary

Klippel-Feil syndrome is a rare condition characterized by a short neck and fused cervical vertebrae. This case report details an 8-year-old boy diagnosed with this syndrome due to his symptoms.

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Area of Science:

  • Genetics
  • Orthopedics
  • Pediatrics

Background:

  • Short neck and cervical vertebrae fusion are hallmarks of various genetic disorders and syndromes.
  • Klippel-Feil syndrome is a congenital condition affecting the cervical spine.

Observation:

  • An 8-year-old boy presented with a short neck, low-set posterior hairline, and hearing loss.
  • Limited neck motion was also noted in the patient.

Findings:

  • Clinical examination and radiographic imaging confirmed the diagnosis.
  • The patient was diagnosed with Klippel-Feil syndrome.

Implications:

  • This case highlights the importance of recognizing Klippel-Feil syndrome in pediatric patients with characteristic symptoms.

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  • Early diagnosis aids in managing associated complications and providing appropriate care.