Three Cases of Familial Occurrence of Crouzon's Disease (Cranlofaeial Dysostosis)
Journal of the Korean Ophthalmological Society
;
: 651-656, 1980.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Prognathism
/
Exophthalmos
/
Exotropia
/
Family Characteristics
/
Craniofacial Dysostosis
Limits:
Humans
Language:
Korean
Journal:
Journal of the Korean Ophthalmological Society
Year:
1980
Type:
Article
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