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Crouzon syndrome

Optometry - Journal of the American Optometric Association, 2006
Crouzon syndrome is a rare genetic disorder characterized by distinctive malformations of the skull and facial region. Premature cranial suture closure is the most common skull abnormality. Optic disc edema and proptosis are among the most common ocular findings.We present a case of a 5-year-old girl with Crouzon syndrome displaying classic facial ...
Ernest L, Bowling, Fernando D, Burstein
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Hydrocephalus in Crouzon's syndrome

Child's Nervous System, 1989
We reviewed 42 cases of Crouzon's syndrome. There were 16 cases with ventricular dilation. We believe that shunt should be inserted after fronto-orbital advancement if there are persistent signs of raised intracranial pressure. However, in cases presenting with severe ventricular dilation and papilloedema, a shunt is inserted prior to fronto-orbital ...
A, Hanieh, R, Sheen, D J, David
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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
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Glaucoma With Crouzon Syndrome

Journal of Glaucoma, 2018
Background:Crouzon syndrome is the most common form of craniosynostosis, and mutations in the fibroblast growth factor receptor 2 and 3 (FGFR2andFGFR3) genes are implicated in its pathogenesis.Observation:A 10-year-old female patient with Crouzon syndrome and congenital glaucoma treated with trabeculectomy and ocular hypotensive medications was ...
Abdulaziz A, Alshamrani   +1 more
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Crouzon’s syndrome

1996
The exact incidence of Crouzon’s syndrome is unknown, but it is a rare condition. However, the incidence of similar conditions which also have abnormalities of the head and face are not uncommon A figure of one in every 2000 children with such abnormalities has been quoted.
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