Abstract
Klippel–Feil syndrome is one of the congenital causes of difficult airway. It is characterised by a classic triad of a short neck, restricted cervical spine movement, and a low posterior hairline, which can pose a significant challenge to the anaesthetist during airway management. A case of Klippel Feil Syndrome type 2 with associated Sprengel’s deformity for panendoscopy under general anaesthesia is presented. The anaesthetic considerations in the management of this patient are also discussed.
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