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.
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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