ArticleJournal of maxillofacial and oral surgery2025
Trifid Epiglottis with Midline Cleft Lip: A Rare Craniofacial Anomaly-First Case Report.
Article in Journal of maxillofacial and oral surgery, 2025. 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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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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5 authors.
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Abstract
Congenital anomalies involving the epiglottis are an uncommon occurrence and are seldom reported as isolated anomalies. Bifid epiglottis, by itself, is also a rare occurrence. Trifid epiglottis has only been reported once in literature to the best of our knowledge. Epiglottic anomalies are observed commonly as part of a syndrome or a sequence, mostly in association with facial dysmorphic features, cleft lip and palate, polydactyly, and skeletal abnormalities among others. We report to you the case of a 10 year-old child having a triad of clinical features consisting of a trifid epiglottis, and a median cleft lip with associated polydactyly.
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