Results 151 to 160 of about 3,732 (189)
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Early operation in craniofacial dysostosis
World Journal of Surgery, 1989AbstractCraniofacial dysostosis is encountered in different congenital malformations such as Kleeblattschädel deformity, Crouzon's disease, and Apert's, Chotzen's, Pfeiffer's, and Carpenter's syndromes. Premature closure of cranial and facial sutures leads to characteristic disfigurement of the skull with orbital and maxillary hypoplasia.
W, Mühlbauer +6 more
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Strabismus in craniofacial dysostosis
Graefe's Archive for Clinical and Experimental Ophthalmology, 1988Ten infants and children who presented with craniofacial dysostosis are discussed; four had Apert's syndrome, four had Crouzon's syndrome, one had Pfeiffer's syndrome, and one had hypertelorism. The follow-up of the patients ranged from 3 months to 7 years, with an average of 19 months.
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Craniofacial dysostosis syndromes: stages of reconstruction
Oral and Maxillofacial Surgery Clinics of North America, 2004The term "craniofacial dysostosis" is used in a general way to describe syndromal forms of craniosynostosis. These disorders are characterized by sutural involvement that not only includes the cranial vault but also extends into the skull base and midfacial skeletal structures.
Jeffrey C, Posnick +2 more
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Crouzon's disease (craniofacial dysostosis)
Journal of Neurosurgery, 1972✓ This article discusses the nature and treatment of Crouzon's disease and reproduces a translation of part of Crouzon's original description. Six typical patients with this disease are presented, and the reasons for surgical treatment emphasized.
J, Kushner +4 more
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[Crouzon's craniofacial dysostosis].
Archivio per le scienze mediche, 2007A brief account of craniofacial synostosis is presented. The cranium is acrocephalic owing to the early closure of the coronal and lambdoid sutures. The crown is typically rudimentary where the anterior fontanel is still open. Cranial radiography shows digitate markings. Skeletal changes lead to hypertelorism, exophthalmos and strabismus.
A, Spada, S, Ambrosiani
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Cranial base dynamics in craniofacial dysostosis
Journal of Maxillofacial Surgery, 1984Cephalometric 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 ...
H M, Rosen, L A, Whitaker
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CRANIOFACIAL DYSOSTOSIS OF CROUZON
Pediatrics, 1959THIS REPORT describes an infant with craniofacial dysostosis noted at birth. As in the original description by Crouzon, the infant demonstrated a bony-hard protrusion of the skull in the region of the anterior fontanelle, with widening of the transverse diameter and anteroposterior shortening.
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[Craniofacial dysostosis with diaphyseal hyperplasia].
Journal de genetique humaine, 1982The only family known so far to have developed cranio-facial dysostose, has been the object of a new study. Since 1962, 3 new infants affected by this disease were born and another 3 died. The syndrome is characterized by an important growth deficit, small cranium with thin skull bone, a peculiar facies with marked hypoplasia of the middle portion and ...
C, Maximilian +6 more
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Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1973
A P, Romodanov, D S, Liashchenko
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A P, Romodanov, D S, Liashchenko
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