Three Cases of Familial Occurrence of Crouzon's Disease (Cranlofaeial Dysostosis)
Journal of the Korean Ophthalmological Society
;
: 651-656, 1980.
Artículo
en Coreano
| WPRIM
| ID: wpr-25553
ABSTRACT
Craniofacial dysostosis, a well defined. rare syndrome first described by Crouzon in 1912, characteristically shows frontal bosses, prognathism, exophthalmos, exotropia, optic nerveatrophy and maxillary hypoplasia. Three cases of familial occurrence are presented, and according to their history, 11 of 13 members in 5 generations of their family are suspected to have been afflicted. A brief review of related literature is described.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Prognatismo
/
Exoftalmia
/
Exotropía
/
Composición Familiar
/
Disostosis Craneofacial
Límite:
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Año:
1980
Tipo del documento:
Artículo
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