ArticleBMJ case reports2018
Cerebrofacial arteriovenous metameric syndrome with hypopituitarism: a rare association.
Article in BMJ case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 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
4 citing papers in PubMed, 2 citations in OpenAlex.
- Cerebrofacial arteriovenous metameric syndrome: Case report and brief literature review.Journal of vascular surgery cases and innovative techniques · 2026Article
- Assuming the right approach in cerebrofacial arteriovenous metameric syndrome: a case report.Croatian medical journal · 2026Article
- Cerebrofacial arteriovenous metameric syndrome type I + II + III: An unusual case.Clinical case reports · 2024Article
- The cerebrofacial metameric syndromes: An embryological review and proposal of a novel classification scheme.Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences · 2022Review
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Case of cerebrofacial arteriovenous metameric syndrome (CAMS) in a 9-year-old boy is described with arteriovenous malformation simultaneously involving the brain and face, with characteristic CAMS type 1 and 2 involvement. This patient demonstrates the wide spectrum of clinical manifestations of CAMS, and in this particular case, the patient exhibits features of hypopituitarism-an association that was not previously described in the literature to our knowledge. Awareness of the underlying embryological abnormality and recognition of resultant clinical and radiological presentations are paramount for diagnosis and treatment.
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Registered trials
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