ArticleWorld journal of clinical cases2018
Carney complex: Two case reports and review of literature.
Article in World journal of clinical cases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 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.
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Who cites it
9 citing papers in PubMed, 16 citations in OpenAlex.
- From misclassified AIP variant to carney complex: a case report and retrospective evaluation of PRKAR1A in pituitary tumor predisposition.Pituitary · 2025Article
- Nasal Osteochondromyxoma Without Carney Complex: A Case Report and a Literature Review.Cureus · 2024Article
- An adolescent case of sellar osteochondromyxoma in the setting of spondyloepiphyseal dysplasia.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023Article
- Trigeminal Nerve Melanotic Schwannoma in Carney Complex.The Indian journal of radiology & imaging · 2022Article
- Article
- Dermatological and endocrine elements in Carney complex (Review).Experimental and therapeutic medicine · 2021Review
- Recurrent Atrial Myxoma in a Patient with Carney Complex. A Case Report and Literature Review.Arquivos brasileiros de cardiologia · 2020Review
- Obstetric and Neonatal Outcome of Pregnancy in Carney Complex: A Case Report.Frontiers in endocrinology · 2020Article
- Ring sign: an imaging sign for osteochondromyxoma in Carney complex.Quantitative imaging in medicine and surgery · 2019Article
Corrections and comments
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Carney complex (CNC) is an extremely rare genetic syndrome of pigmented skin lesions, endocrine hyperfunction and myxoma. Given its diverse clinical manifestations, CNC is often misdiagnosed. Recognition of some special clinical manifestations and imaging features may help with the diagnosis. Early diagnosis of CNC would alert ongoing surveillance of tumors and complications; the prognosis of CNC may thus be improved by early treatment. Herein, we report two cases of CNC with bone lesions.
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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.