ArticleJournal of clinical medicine2023
Jacob's Disease: Case Series, Extensive Literature Review and Classification Proposal.
Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Endoscopically Assisted Management of Bilateral Coronoid Hyperplasia: A Case Report with Oral-Health-Related Quality of Life Outcomes.Journal of clinical medicine · 2026Article
- Cone Beam Computed Tomography Evaluation and Proposal of a Functional Radiographic Classification of the Coronoid Process-A Cross-Sectional Study.Journal of clinical medicine · 2025Article
- Reply to Mattei et al. Jacob Disease, Osteochondroma of the Coronoid Process, Coronoid Process Hyperplasia or Langenbeck Disease: The Big Jumble. Comment on "Raccampo et al. Jacob's Disease: Case Series, Extensive Literature Review and Classification Proposal.Journal of clinical medicine · 2023Article
- Jacob Disease, Osteochondroma of the Coronoid Process, Coronoid Process Hyperplasia or Langenbeck Disease: The Big Jumble. Comment on Raccampo et al. Jacob's Disease: Case Series, Extensive Literature Review and Classification Proposal.Journal of clinical medicine · 2023Article
- Temporomandibular Joint Disorders: Functional and Conservative Treatment.Journal of clinical medicine · 2023Article
- Article
- Spontaneous Zygomatic Remodelling after Coronoidectomy in Coronoid Process Hyperplasia and Jacob's Disease - A Case Report and Literature Review.Annals of maxillofacial surgeryArticle
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Jacob's disease is a rare entity consisting of the formation of a pseudojoint between an abnormal coronoid process of the mandible and the inner surface of the zygomatic bone. First described by Jacob in 1899, its diagnosis and definition have never been entirely univocal. In this paper, we present three emblematic cases and an extensive review of the literature on Jacob's disease. Given the variability observed in the presentation of the disease, we have developed a proposal for the classification, here reported.
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Registered trials
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