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. 2023 May 1;34(3):e330-e331.
doi: 10.1097/SCS.0000000000009259. Epub 2023 Mar 13.

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

Affiliations

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

Mark S Shafarenko et al. J Craniofac Surg. .

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.

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Conflict of interest statement

The authors report no conflicts of interest.

References

    1. Merenzon MA, Dorman MA, Zuliani Sampaolesi P, et al. Case report of worth syndrome and Chiari I malformation: unusual association and surgical treatment. World Neurosurg 2018;115:225–228
    1. Payne K, Dickenson A. Worth syndrome as a diagnosis for mandibular osteosclerosis. Dentomaxillofac Radiol 2011;40:531–533
    1. Thompson KS, Owosho AA. Worth syndrome “mandibular osteosclerosis” as an incidental finding: a report of 2 cases. Dentomaxillofac Radiol 2018;47:20180171
    1. Gorlin R, Glass L. Autosomal dominant osteosclerosis. Radiology 1977;125:547–548
    1. Worth HM, Wollin D. Hyperostosis corticalis generalisata congenita. J Can Assoc Radiol 1966;17:67–74

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