[Syndromes 11. Treacher collins syndrome]. / Syndromen 11. Syndroom van Treacher Collins.
Ned Tijdschr Tandheelkd
; 106(6): 226-8, 1999 Jun.
Article
en Nl
| MEDLINE
| ID: mdl-11930479
Treacher Collins syndrome is seen once in 10.000 births. Inheritance is autosomal dominant with variable expressivity. The most prominent symptoms are antimongoloid slant of the eyelids, hypo- or even aplasia of the zygomata, very hypoplastic mandible with receding chin, deformed ear lobes and conductive hearing loss. With two to three operations a considerable improvement can be achieved. The correction of the eyelids is often the most difficult problem.
Buscar en Google
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Pérdida Auditiva Conductiva
/
Disostosis Mandibulofacial
Límite:
Humans
Idioma:
Nl
Revista:
Ned Tijdschr Tandheelkd
Año:
1999
Tipo del documento:
Article
Pais de publicación:
Países Bajos