Abbe flap: a pedicled full thickness flap of one lip transferred into the other
Addison disease: chronic adrenal insufficiency, hypocortisolism, hypoadrenalism, and buccal mucosa pigmentation
Adson tissue forceps
Albers-Schonberg disease: osteopetrosis
Albright syndrome: precocious puberty, polyostotic fibrous dysplasia, unilateral café-au-lait spots
Allen’s test for radial or ulnar artery patency
Apert’s syndrome: type I acrocephalosyndactyly
Battle’s sign: post-auricular ecchymosis in # of middle cranial fossa
Behçet’s syndrome: uveitis, oral, and genital ulceration
Bell’s palsy: idiopathic unilateral facial nerve paralysis, usually self-limiting
Binder’s syndrome: nasomaxillary hypoplasia
Bowen’s disease: cutaneous squamous intra-epithelial carcinoma
Breslow thickness: melanoma depth
Burkitt’s lymphoma: EBV in African children
Caldwell–Luc approach via canine fossa to maxillary sinus
Carnoy’s solution: a fixative used in keratocystic odontogenic tumour management
Castleman disease: uncommon lympho-proliferative disorder (not reactive lymph node hyperplasia or malignancy)
Chvostek’s sign: hypocalcaemia-related tapping over facial nerve elicits abnormal muscle contraction(s)
Crohn’s disease: inflammatory bowel disease, may affect any part of the gastrointestinal tract from mouth to anus
Crouzon syndrome: craniofacial dysostosis
Di George syndrome: deficiency of 3rd and 4th pharyngeal pouches, cellular immunodeficiency, overlap with VCF
Epstein’s pearls: cystic papules on palate
Erb’s point: where the great auricular nerve crosses the SCM
Abbe–Estlander flap: a full thickness flap reconstruction of oral commissure
Weber–Fergusson incision: facial access for maxillectomy
Frey’s syndrome: gustatory sweating following parotid surgery or trauma
Gardner’s syndrome: variant of familial adenomatous polyposis with osteomas, neuromas, lipomas, polyposis coli
Gillies lift: surgical approach to closed zygomatic fracture reduction
Also needle holder, tissue forceps, skin hooks
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