Evidence map›Paper›PMID 38440616›Full record

ArticleIndian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India2024

Gorlin-Goltz Syndrome: An Incidental Finding of a Rare Entity.

Sugandha Verma, Sri Krishna Koppula, Devarshi Nandi, Vikas Kumar

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In one paragraph

Article in Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 70% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Sugandha VermaOral Medicine and Radiology, Dental Institute, Rajendra Institute of Medical Sciences (RIMS), Ranchi, Jharkhand 834009 India.ORCID 0000-0002-3638-5868
Sri Krishna KoppulaOral Medicine and Radiology, Hazaribagh College of Dental Sciences and Hospital, Demotand, Hazaribagh, 825301 India.
Devarshi NandiOral Medicine and Radiology, Hazaribagh College of Dental Sciences and Hospital, Demotand, Hazaribagh, 825301 India.
Vikas KumarOral Medicine and Radiology, Dental Institute, Rajendra Institute of Medical Sciences (RIMS), Ranchi, Jharkhand 834009 India.ORCID 0009-0006-9781-0916
Rajendra Institute of Medical Sciences · INVinoba Bhave University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gorlin-Goltz syndrome (GGS) is a rare hereditary disease characterized by multiple basal cell carcinomas, odontogenic keratocyst (OKCs) and musculoskeletal malformations. Pathogenesis of the syndrome is attributed to abnormalities in the long arm of chromosome 9 (q22.3-q31) and mutations in the human patched gene (PTCH1 gene). Here, we report a rare case of an incidental finding of GGS in an 18-year-old male patient presenting multiple OKCs, calcification of the falx cerebri, and bifid rib.

Indexed as

Bifid ribGorlin–Goltz syndromeKeratocystic odontogenic tumorOdontogenic keratocyst

Identifiers

PMID38440616
PMCPMC10909011
OpenAlexW4387654519

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.