Frontonasal dysplasia: A case report
Archives of Craniofacial Surgery
;
: 397-400, 2019.
Artículo
en Inglés
| 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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Fenotipo
/
Hipertelorismo
Límite:
Humanos
Idioma:
Inglés
Revista:
Archives of Craniofacial Surgery
Año:
2019
Tipo del documento:
Artículo
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