ArticleCase reports in dentistry2012
Gorlin-goltz syndrome.
Article in Case reports in dentistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 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
7 citing papers in PubMed, 18 citations in OpenAlex.
- An Easily Missed But Life-Threatening Diagnosis: A Case Report of Gorlin Syndrome.The American journal of case reports · 2023Article
- Development of mediastinal lymphoma after radiotherapy for concurrent medulloblastoma and PNET in a patient with Gorlin syndrome.World journal of surgical oncology · 2016Article
- Gorlin-Goltz syndrome: A case series of 5 patients in North Indian population with comparative analysis of literature.Contemporary clinical dentistry · 2015Article
- A case of Gorlin-Goltz syndrome presented with psychiatric features.Behavioural neurology · 2014Article
- Gorlin syndrome: A rare case report.Journal of oral and maxillofacial pathology : JOMFPArticle
- Imaging of Gorlin-Goltz syndrome: Series of 2 cases.Journal of oral and maxillofacial pathology : JOMFPArticle
- Gorlin-Goltz Syndrome: Report of a Rare Case with an Update on the Review of the Literature.Contemporary clinical dentistryArticle
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The Gorlin-Goltz syndrome (GGS) (the nevoid basal cell carcinoma syndrome-NBCCS) is a rare autosomal dominant syndrome caused due to mutations in the PTCH (patched) gene found on chromosome arm 9q. The syndrome, characterized by increased predisposition to develop basal cell carcinoma and associated multiorgan anomalies, has a high level of penetrance and variable expressiveness. GGS is a multidisciplinary problem, early diagnosis of which allows introduction of secondary prophylaxis and following an appropriate treatment to delay the progress of the syndrome. The following report emphasizes the need for awareness of the diagnostic criteria of this syndrome in cases with no typical skin lesions.
Identifiers
What 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.