Results 151 to 160 of about 2,768 (208)

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.
Marshall M Parks, Frank D Costenbader
exaly   +5 more sources

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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.
C Lauritzen
exaly   +3 more sources

Cranial base dynamics in craniofacial dysostosis

Journal of Maxillofacial Surgery, 1984
Cephalometric analyses of twenty-one patients with Crouzon's disease were undertaken to correlate the cranial base abnormalities to altered facial morphology. Angular deformities of the cranial base, i.e., the vertical sloping of the anterior cranial fossa and the angulation of the cranial base flexure were found to correlate well to observed ...
Harvey M Rosen, Linton A Whitaker
exaly   +3 more sources

Craniofacial Dysostosis With Syringomyelia and Associated Anomalies

Archives of Neurology, 1976
A 16-year old boy had craniofacial dysostosis, hydrocephalus, and syringomyelia. Other anomalies included platybasia, a Klippel-Feil anomaly, webbed toes, and a cutaneous hemangioma. Evaluation included cerebral angiography, ventriculography, and myelography.
J P, Berke, K R, Magee
exaly   +3 more sources

Absence of Superior Recti in Craniofacial Dysostosis

JAMA Ophthalmology, 1965
Premature synostosis of cranial bones has prompted the description of multiple clinical entities such as craniofacial dysostosis (Crouzon's Disease), acrocephalosyndactylia (Apert's disease), oxycephaly, and many others. The main ocular findings described in these syndromes have been shallowing of the orbits with orbital divergence, exotropia without ...
F J, WEINSTOCK, H H, HARDESTY
exaly   +3 more sources

Craniofacial Dysostosis

Neurosurgery Clinics of North America, 1991
Jeffrey C Posnick
exaly   +2 more sources

The Craniofacial Dysostosis Syndromes

Clinics in Plastic Surgery, 1994
Jeffrey C Posnick
exaly   +2 more sources