Crouzon syndrome with acanthosis nigricans: A case report and literature review [PDF]
Dermatology Reports, 2022 Crouzon’s syndrome with acanthosis nigricans is an autosomal dominant disease, with typical features of classic Crouzon craniosynostosis, verrucous hyperplasia, and hyperpigmentation of the skin.
Quan Duy Nguyen +2 more
doaj +2 more sources
Computed tomography findings of Crouzon syndrome: A case report [PDF]
Radiology Case Reports, 2022 Crouzon syndrome is a genetic condition characterized by a premature fusion of skull sutures resulting in head and facial deformities. Crouzon syndrome is usually suspected at birth through physical examination or in the antenatal period via ...
Juan Guillermo Arámbula Neira, MD +6 more
doaj +2 more sources
Crouzon syndrome and the eye: An overview [PDF]
Indian Journal of Ophthalmology, 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
Kasturi Bhattacharjee +7 more
doaj +2 more sources
Crouzon Syndrome Spanning Three Generations: Advances in the Treatment of Syndromic Midface Deficiency [PDF]
Plastic and Reconstructive Surgery, Global Open, 2023 Background:. Crouzon syndrome is an autosomal dominant genetic disorder characterized by craniosynostosis, midface retrusion, and exophthalmos. Over the past century, the treatment of craniofacial disorders like Crouzon syndrome has evolved significantly.
Kelly A. Harmon, BS +5 more
doaj +2 more sources
Clues from Crouzon: Insights into the potential role of growth factors in the pathogenesis of myelinated retinal nerve fibers [PDF]
Journal of Current Ophthalmology, 2016 Purpose: We present a case of bilateral extensive peripapillary myelinated retinal nerve fibers (MRNF) in an individual with Crouzon syndrome, an inherited form of craniosynostosis caused by overactivation of fibroblast growth factor receptor 2.
Giancarlo A. Garcia +5 more
doaj +5 more sources
FGFR2 Mutation p.Cys342Arg Enhances Mitochondrial Metabolism-Mediated Osteogenesis via FGF/FGFR-AMPK-Erk1/2 Axis in Crouzon Syndrome [PDF]
Cells, 2022 Background: Crouzon syndrome ([OMIM] #123500) caused by FGFR2 mutation is an autosomal dominant syndrome with craniosynostosis, the underlying mechanism of which remains obscure.
Yidi Wang +6 more
doaj +2 more sources
Crouzon syndrome complicated with binocular strabismus and extraocular muscle fibrosis: a case report [PDF]
Journal of Medical Case Reports, 2023 Background Crouzon syndrome, a rare genetic disorder characterized by premature closure of coronal sutures, results in skull and facial deformities along with abnormal brain and ocular development.
Yuling Niu +5 more
doaj +2 more sources
Cranial Base Reconstruction and Secondary Frontal Advancement for Meningoencephalocele Following LeFort III Osteotomy in a Patient with Crouzon Syndrome: Case Report [PDF]
Archives of Plastic Surgery, 2023 Patients with Crouzon syndrome have increased risks of cerebrospinal fluid rhinorrhea and meningoencephalocele after LeFort III osteotomy. We report a rare case of meningoencephalocele following LeFort III midface advancement in a patient with Crouzon ...
Sungmi Jeon +3 more
doaj +2 more sources
Contemporary Clinical Dentistry, 2010 Crouzon syndrome is an autosomal dominant condition of the craniosynostotic syndromes without syndactyly and with various dentofacial anomalies.
Y Samatha +4 more
doaj +3 more sources
Progressive myelinated retinal nerve fibers in a 10-year-old boy with Crouzon syndrome after craniofacial surgery [PDF]
American Journal of Ophthalmology Case Reports, 2023 Purpose: We present a case of a 10-year-old boy with Crouzon syndrome that demonstrates progressive myelinated retinal nerve fibers (MRNF). Observations: A 10-year-old boy was referred for ophthalmic examination due to clusters of opaque white fibers ...
Norman A. Saffra +3 more
doaj +2 more sources