Document Type

Article

Publication Title

Cureus

Abstract

Klippel-Feil syndrome (KFS) is a rare congenital condition characterized by the fusion of cervical vertebrae. It classically presents with a triad of symptoms: limited cervical range of motion, a low posterior hairline, and a short neck. Common otolaryngological manifestations include hearing loss, dysphagia, cleft palate, jaw disorders, thyroid abnormalities, and ear malformations, highlighting the importance of KFS awareness in the field of otolaryngology. Recognizing these symptoms can enhance patient care and outcomes. This systematic review analyzed all case reports on KFS published in the last 10 years on PubMed. Cases were classified using the Samartzis classification, Mallampati score, and Cormack-Lehane grade. Symptoms were then identified, and common imaging techniques were noted to provide clinical recommendations for treating KFS patients. The study found that more severe vertebral fusions are linked to more serious symptoms. Otolaryngologists should consider KFS in their differential diagnosis, especially in patients presenting with neck masses and pain, hearing loss, dysphagia, scoliosis, Sprengel's deformity, or other musculoskeletal abnormalities.

DOI

10.7759/cureus.73986

Publication Date

11-19-2024

Keywords

hearing loss, Klippel-Feil Syndrome, otolaryngology, rare genetic disorder, spinal cord fusion

ISSN

2168-8184

Download

Share

COinS