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Crouzon syndrome and the eye: An overview. [PDF]
Indian J Ophthalmol, 2022 The current literature review aims to evaluate the ocular findings and associated ophthalmic features in Crouzon syndrome. Craniosynostoses are syndromes characterized by premature fusion of sutures of the skull and Crouzon syndrome is the most common of the craniosynostosis syndromes.
Bhattacharjee K +7 more
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Citation: 'Crouzon syndrome' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.10575 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
Zeppieri M, Karsonovich T, Patel BC.
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Clinical characteristics of Crouzon syndrome.
Oman J Ophthalmol, 2017 Crouzon syndrome (CS) is an genetic disorder with autosomal dominant inheritance caused by mutation of the gene for fibroblast growth factor receptor 2 (FGFR2) was described as one of the varieties of craniosynostosis. In this presented case, premature closure of the sutures had caused restricted skull growth and lack of space for the growing brain ...
Balyen L, Deniz Balyen LS, Pasa S.
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Crouzon syndrome: Genetic and intervention review [PDF]
Journal of Oral Biology and Craniofacial Research, 2019 Nisreen Mohammed Al-Namnam +2 more
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Contemporary Clinical Dentistry, 2010 Crouzon syndrome is an autosomal dominant condition of the craniosynostotic syndromes without syndactyly and with various dentofacial anomalies. Craniosynostosis, maxillary hypoplasia, shallow orbits, ocular proptosis and hypertelorism are the characteristic features of Crouzon syndrome.
Y Samatha +4 more
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Delhi Journal of Ophthalmology, 2010 A 27 year old male patient presented with sudden onset of pain, redness, photophobia and diminution of vision in left eye since 10 days, no past history of ocular injury. At presentation visual acuity in right eye was 6/9 and that of left eye was HM +ve, on slit lamp examination corneal ulcer with hypopyon was ...
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Medical Journal of Dr. D.Y. Patil University, 2013 Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Crouzon syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene.
Neha Rajappa +3 more
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Crouzon syndrome: a social stigma [PDF]
BMJ Case Reports, 2012 Crouzon syndrome is a rare genetic disorder caused due to genetic mutations. It is characterised by partial hearing loss, dry eyes, strabismus and underdevelopment of the upper jaw with facial deformities and malocclusion. These facial deformities greatly affect the social and emotional development of the affected child.
Neelisha, Pandey +3 more
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Crouzon syndrome: A comprehensive review [PDF]
Balkan Journal of Dental Medicine, 2018 Crouzon syndrome is a rare genetic disorder with autosomal dominant inheritance. The underlying pathological process is premature synostosis of the cranial sutures with subsequent phenotypic alterations of the affected person. A review of the literature has been conducted in order to resume the overall characteristics of Crouzon syndrome such as ...
Kyprianou Chrystalla +1 more
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