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Frontonasal dysplasia: A case report
Archives of Craniofacial Surgery ; : 397-400, 2019.
Article Dans Anglais | WPRIM | ID: wpr-785444
ABSTRACT
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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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Phénotype / Hypertélorisme Limites du sujet: Humains langue: Anglais Texte intégral: Archives of Craniofacial Surgery Année: 2019 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Phénotype / Hypertélorisme Limites du sujet: Humains langue: Anglais Texte intégral: Archives of Craniofacial Surgery Année: 2019 Type: Article