ArticleJournal of international oral health : JIOH2015
Odontogenic Keratocysts in Gorlin-Goltz Syndrome: A Case Report.
Article in Journal of international oral health : JIOH, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
8 citing papers in PubMed, 12 citations in OpenAlex.
- Clinical manifestations and treatment of peripheral odontogenic keratocysts: two cases and a literature review.Orphanet journal of rare diseases · 2025Review
- Gorlin-Goltz syndrome: Multidisciplinary approach for early diagnosis of rare disease for better patient outcome.Radiology case reports · 2025Article
- Radiological evaluation of odontogenic keratocysts in patients with nevoid basal cell carcinoma syndrome: A review.The Saudi dental journal · 2023Review
- Gorlin-Goltz Syndrome: A Case Series.Cureus · 2023Article
- Basal Cell Nevus Syndrome with Unusual Associated Findings: A Case Report with 17 Years of Follow-Up.The American journal of case reports · 2021Article
- Removal of Multiple Keratocystic Odontogenic Tumors in a Nonsyndromic Patient.Annals of maxillofacial surgeryArticle
- Gorlin-Goltz Syndrome: A Rare Case Report.Contemporary clinical dentistryArticle
- Neonatal Onset Glaucoma in a Case with Gorlin-Goltz Syndrome: An Unusual Association.Journal of current glaucoma practiceArticle
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Gorlin-Goltz syndrome is an autosomal dominant inherited condition comprising the principle triad of basal cell carcinomas, multiple jaw keratocysts, and skeletal anomalies. The presence of jaw cysts are the early diagnostic feature of this syndrome, and this can be incidentally identified by routine radiographs. A patient presented with signs and symptoms of Gorlin-Goltz syndrome to us in her early stages.
Indexed as
Identifiers
26225111PMC4516062W2415826387What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.