Three Cases of Familial Occurrence of Crouzon's Disease (Cranlofaeial Dysostosis)
Journal of the Korean Ophthalmological Society
;
: 651-656, 1980.
Article
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Prognathisme
/
Exophtalmie
/
Exotropie
/
Caractéristiques familiales
/
Dysostose craniofaciale
Limites du sujet:
Humains
langue:
Coréen
Texte intégral:
Journal of the Korean Ophthalmological Society
Année:
1980
Type:
Article
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