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Multidisciplinary management of Crouzon syndrome
The Journal of the American Dental Association, 1979The comprehensive management of Crouzon syndrome in a 14-year-old girl has been presented. Because of the complexity of the facial and associated problems, a multidisciplinary approach is necessary to provide maximum functional and esthetic results; however, with such a cooperative interdisciplinary effort, the improvement and benefits derived for ...
T A, Turvey, R E, Long, D J, Hall
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Ophthalmic Sequelae of Crouzon Syndrome
Ophthalmology, 2005To document the frequency of ophthalmic sequelae in patients with Crouzon syndrome before the influence of craniofacial surgery.Retrospective observational case series.Seventy-one consecutive patients with a clinical diagnosis of Crouzon syndrome assessed before craniofacial or ophthalmic surgery at the Australian Craniofacial Unit between 1984 and ...
Gray, T. +4 more
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Germinal mosaicism in Crouzon syndrome
Human Genetics, 1990Two sibs with classic Crouzon syndrome of the same mother but different fathers are presented as an example of germinal mosaicism in a known autosomal dominant disorder. The mother and both fathers were completely normal.
S, Kreiborg, M M, Cohen
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Hand anomalies in Crouzon syndrome
Skeletal Radiology, 1997To review the hand radiographs of patients with Crouzon syndrome, to look for extracranial manifestations of the condition at this site.The hand radiographs of those with Crouzon syndrome attending the Craniofacial Service at Great Ormond Street between 1985 and 1996 were reviewed.Thirty-three patients underwent a total of 34 radiographs, one patient ...
P J, Anderson +4 more
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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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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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Germinal mosaicism in Crouzon syndrome
Clinical Genetics, 1988Two brothers with Crouzon craniofacial dysostosis syndrome born to normal unrelated parents are described. Paternity studies show the probability of paternity is 99.6%. This report appears to represent the first example of germinal mosaicism in Crouzon syndrome.
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Integrative oncology: Addressing the global challenges of cancer prevention and treatment
Ca-A Cancer Journal for Clinicians, 2022Jun J Mao,, Msce +2 more
exaly