ArticleIn vivo (Athens, Greece)
Phenotype and Surgical Treatment in a Case of Proteus Syndrome With Craniofacial and Oral Findings.
Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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Who cites it
1 citing paper in PubMed.
- Proteus syndrome with late diagnosis confirmation: a case report.Frontiers in pediatrics · 2025Article
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1 author.
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Abstract
BACKGROUND/
aimProteus syndrome is a sporadic disease that is particularly noticeable due to the disproportional growth of body segments. The disease is a genetic mosaic. The mutations can arise from any of the germ layers, an explanation of the very variable phenotype. The aim of this report is to communicate the diagnosis and management of an unusual case of Proteus Syndrome with special attention to oral and craniofacial findings. CASE REPORT: A 15-year-old patient was referred for surgical treatment of pronounced skull malformations and correction of oral mucosal hyperplasia. Treatment caused significant improvement in facial appearance and oral soft tissue conditions.
conclusionSurgical measures adapted to the local findings and symptoms can often relieve severe disfigurement of the patient.
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