Abstract
Klippel-Feil syndrome (KFS) is a rare condition also known as synostosis of cervical spine, first described in the medical literature in 1912. It consists of the triad of symptoms such as short neck, limitation of neck movements, and low posterior hairline and also associated with somatic diseases and defects such as scoliosis, anomalies in urogenital system, congenital heart defects, deafness, facial asymmetry, synkinesis, or mirror movements. KFS manifests in the oral cavity with cleft palate, limitation of mouth opening, hypodontia oligodontia, and micrognathia.
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