Worth Syndrome—Patient Report, Diagnostic Work-Up, and Surgical Management of a Rare Craniofacial Entity

Author:

Shafarenko Mark S.1,Klieb Hagen B.2,Antonyshyn Oleh M.13

Affiliation:

1. The Division of Plastic and Reconstructive Surgery, Department of Surgery, University of Toronto

2. Department of Dentistry, Sunnybrook Health Sciences Centre

3. Division of Plastic and Reconstructive Surgery, Sunnybrook Health Sciences Centre, Toronto, ON

Abstract

Worth syndrome is a rare genetic bone disorder that often presents with cortical thickening of the mandible and an increase in mandibular width. The authors report the preoperative considerations in a young female with Worth syndrome, operative planning, and successful mandibular reduction using cutting guides.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Otorhinolaryngology,Surgery

Reference6 articles.

1. Case report of worth syndrome and Chiari I malformation: unusual association and surgical treatment;Merenzon;World Neurosurg,2018

2. Worth syndrome as a diagnosis for mandibular osteosclerosis;Payne;Dentomaxillofac Radiol,2011

3. Worth syndrome “mandibular osteosclerosis” as an incidental finding: a report of 2 cases;Thompson;Dentomaxillofac Radiol,2018

4. Autosomal dominant osteosclerosis;Gorlin;Radiology,1977

5. Hyperostosis corticalis generalisata congenita;Worth;J Can Assoc Radiol,1966

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