Results 171 to 180 of about 3,768 (222)
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Craniofacial Dysostosis (Crouzon's Disease)

American Journal of Ophthalmology, 1950
CRANIOFACIAL dysostosis, a rare deformity, produced by premature synostosis of certain craniofacial sutures, characteristically shows frontal bosses, prognathism, exophthalmos, exotropia, optic nerve atrophy and maxillary hypoplasia and, as will be shown, is a dominant hereditary character.
M M, PARKS, F D, COSTENBADER
openaire   +3 more sources

CRANIOFACIAL DYSOSTOSIS: CROUZON'S DISEASE

Pediatrics, 1959
IN 1912 Crouzon presented his classic paper to the Medical Society of the Hospitals of Paris. It was a report on two patients, a 29-year-old mother and her 3-year-old son, with strange malformations of the face and head to which he gave the name "hereditary craniofacial dysostosis." In general Crouzon listed the following factors as characteristic of ...
H W, DODGE, M W, WOOD, R L, KENNEDY
openaire   +2 more sources

Craniofacial Dysostosis: Airway Obstruction and Craniofacial Surgery

Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery, 1996
Craniofacial surgery in craniofacial dysostosis on airway obstruction was studied retrospectively in a consecutive series of patients. The records of 76 patients were reviewed, 27 with Apert syndrome, 47 with Crouzon's syndrome, and two with Pfieffer's syndrome.
M, Järund, C, Lauritzen
openaire   +2 more sources

Hereditary Craniofacial Dysostosis

American Journal of Ophthalmology, 1941
openaire   +1 more source

Crouzon Craniofacial Dysostosis

2009
Nils Peters   +199 more
openaire   +1 more source

Craniofacial Dysostosis Syndromes

2012
Jeffrey C. Posnick   +2 more
openaire   +1 more source

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