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KMID : 1033720190200060397
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Archives of Craniofacial Surgery
2019 Volume.20 No. 6 p.397 ~ p.400
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Frontonasal dysplasia: A case report
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Lee Se-Il
Lee Seung-Je
Joo Hong-Sil
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Abstract
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Frontonasal dysplasia is an uncommon congenital anomaly with diverse clinical phenotypes and highly variable clinical characteristics, including hypertelorism, a broad nasal root, median facial cleft, a missing or underdeveloped nasal tip, and a widow’s peak hairline. Frontonasal dysplasia is mostly inherited and caused by the ALX genes (ALX1, ALX3, and ALX4). We report a rare case of a frontonasal dysplasia patient with mild hypertelorism, a broad nasal root, an underdeveloped nasal tip, an accessory nasal tag, and a widow’s peak. We used soft tissue re-draping to achieve aesthetic improvements.
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KEYWORD
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Frontonasal dysplasia, Frontorhiny, Median facial cleft
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