ArticleImaging science in dentistry2012
Radiological features of familial Gorlin-Goltz syndrome.
Article in Imaging science 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.
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Who cites it
7 citing papers in PubMed, 17 citations in OpenAlex.
- An enigma of Gorlin-Goltz syndrome: Two cases reported in mother and daughter.Journal of oral and maxillofacial pathology : JOMFP · 2019Article
- Gorlin-Goltz syndrome: A case series of 5 patients in North Indian population with comparative analysis of literature.Contemporary clinical dentistry · 2015Article
- Odontogenic Keratocysts in Gorlin-Goltz Syndrome: A Case Report.Journal of international oral health : JIOH · 2015Article
- Gorlin-Goltz syndrome: a rare case report.BMJ case reports · 2013Article
- Radiographic assessment of a keratocystic odontogenic tumour using cone-beam computed tomography.European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry · 2013Article
- Bilateral inflammatory cysts of the jaw: report of an unusual case.Imaging science in dentistry · 2012Article
- 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
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Gorlin-Goltz syndrome is an autosomal dominant disorder principally characterized by cutaneous basal cell carcinomas, multiple keratocystic odontogenic tumors, and skeletal anomalies. This syndrome may be diagnosed early by dentist because keratocystic odontogenic tumors are usually one of the first manifestations of the syndrome. Early diagnosis and treatment are of utmost importance in reducing the severity of long term sequelae of this syndrome. This report presents a rare event of Gorlin-Goltz syndrome occurring in a 39-year-old male and his 8-year-old daughter. The clinical and investigative features of this familial disorder has been described in detail.
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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.