10 LIBRI IN INGLESE ASSOCIATI CON «OCULAR PROPTOSIS»
Scopri l'uso di
ocular proptosis nella seguente selezione bibliografica. Libri associati con
ocular proptosis e piccoli estratti per contestualizzare il loro uso nella letteratura.
1
Syndromes of the Head and Neck
Crouzon syndrome (craniofacial dysostosis) Crouzon syndrome is characterized
by craniosynostosis, maxillary hypoplasia, shallow orbits, and ocular proptosis (
Fig. 14–5). First described by Crouzon (12) in 1912, eighty-six published cases ...
M.S. D.Sc. Regents' Professor Emeritus of Oral Pathology and Genetics at School of Dentistry Robert J. Gorlin D.D.S, D.M.D. M. Michael Cohen Jr., Ph.D. Professor Oral Pathology Faculty of Denistry, Ph.D. Department of Pediatrics and Medical Genetics Raoul C.M. Hennekam M.D., Academic Medical Center University of Amsterdam, 2001
2
The Cat: Clinical Medicine and Management
Ocular proptosis isseenless commonly in catsthan in dogs, likely because of cats'
deep orbitsand relatively tightly fittingadnexa. For this reason theamount of force
requiredtodisplace the globefromthe feline orbitis large, and catswith ocular ...
3
Hereditary Hearing Loss and Its Syndromes
CROUZON SYNDROME (CRANIOFACIAL DYSOSTOSIS) Crouzon syndrome,
characterized by craniosynostosis, maxillary hypoplasia, shallow orbits, and
ocular proptosis, was first described by Crouzon (10) in 1912, and 86 published
cases ...
Helga V. Toriello, Shelley D. Smith, 2013
4
Essentials of Veterinary Ophthalmology
Examples of such causes include injury to the optic nerve during traumatic ocular
proptosis, traction-related damage to the optic nerve at the level of the optic
chiasm during enucleation of the contralateral eye, or previous episodes of optic
...
5
Principles and Practice of Orthognathic Surgery
Jeffrey C. Posnick. Crouzon Syndrome Crouzon syndrome is characterized by
craniosynostosis, maxillary hypoplasia, shallow orbits, and ocular proptosis.* (
Figs. 30-6 through 30-11). Most cases are associated with brachycephaly
secondary ...
6
Perspectives on the Face
Autosomal recessive, COH1 mutations (8q22-q23) Ocular proptosis. See Chapter
5 for etiologv Autosomal recessive. FRAS1 mutations (4q21) Orbital cysts,
microphtlialmia, colobomas. All cases sporadic, to date Keratoglobus, other
ocular ...
Meyer Michael Cohen, 2006
I. The main clinical manifestation of orbital disease is exophthalmos (ocular
proptosis), the extent and direction of which depend on a number of factors*: (1)
size of lesion; (2) character of lesion (expansile versus infiltrative growth, rapid
versus ...
Myron Yanoff, Joseph W. Sassani, 2009
8
Anesthesia and Uncommon Diseases: Expert Consult – Online ...
... may have increased ICP Other: obesity Coronal and others CROUZON'S
SYNDROME Coronal, lambdoid, others HEENT: frontal bossing, tower skull,
midface hypoplasia, beaked nose, hypertelorism, ocular proptosis; airway
obstruction can ...
9
Cefaleas de Origen
Ocular: Un Reto Diagnóstico Y Terapéutico
•A la trombosis del seno cavernoso: dolor ocular, proptosis, inflamación,
oftalmoplejía, dolor y fiebre. •A la fístula carótido-cavernosa: dolor ocular
moderado, hipertensión ocular, a veces oftalmoplejía, inyección conjuntival y
paresias del VI ...
C Compromised airway requir- ing tracheostomy. D Pronounced ocular proptosis
and hypertelorism. E Subluxation ofthe eyeglobe. Crouzon Syndrome Our study
of Crouzon syndrome comprises 61 cases in over 16 published articles [2, 44].
M. Muenke, W. Kress, H. Collmann, 2011