Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Shallow orbits"'
Publikováno v:
GMS Ophthalmology Cases, Vol 14, p Doc04 (2024)
Spontaneous globe subluxation (SGS) is an uncommon condition wherein the equator of the globe protrudes anteriorly beyond the eyelid aperture causing severe lagophthalmos, proptosis and exposure keratopathy. SGS can lead to an emotional disturbance l
Externí odkaz:
https://doaj.org/article/cd40b11f48514fbab7d5c75814e10e8c
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-7 (2023)
Abstract 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. Case presentation Here, we report a case of
Externí odkaz:
https://doaj.org/article/d477a6a7e6094074a924feb979a000e4
Akademický článek
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Autor:
Agustín Martín-Clavijo, Álvaro Bengoa-González, Elena Salvador, Enrique Mencía-Gutiérrez, María-Dolores Lago-Llinás, Bianca-Maria Laslӑu
Publikováno v:
Orbit. 39:190-196
Purpose: To share our experience on deep lateral wall rim-sparing orbital decompression for the prevention of further spontaneous globe subluxation, in patients with shallow orbits and eyelid laxit...
Autor:
Jesse A. Taylor, Youssef Tahiri
Publikováno v:
Seminars in Plastic Surgery. 28:184-192
Le Fort II and III distraction osteogenesis (DO) is a powerful tool in the craniofacial armamentarium that is most often employed to treat patients with craniofacial syndromes such as Crouzon, Apert, or Pfeiffer syndrome who present with midfacial re
Autor:
Karel G.H. van der Wal, Maarten J. Koudstaal, Eppo B. Wolvius, Erik Nout, Jifke F. Veenland, Wim C. J. Hop, Jine S. van Bezooijen
Publikováno v:
Journal of Cranio-Maxillofacial Surgery, 40(3), 223-228. Churchill Livingstone
Patients with syndromic craniosynostosis suffering from shallow orbits due to midface hypoplasia can be treated with a Le Fort III advancement osteotomy. This study evaluates the influence of Le Fort III advancement on orbital volume, position of the
Publikováno v:
Contemporary Clinical Dentistry
Contemporary Clinical Dentistry, Vol 1, Iss 4, Pp 277-280 (2010)
Contemporary Clinical Dentistry, Vol 1, Iss 4, Pp 277-280 (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 charac
Autor:
Sara Osimani, Andrew E. Fry, Koenraad Devriendt, Débora Romeo Bertola, Marjan M. Nezarati, Han G. Brunner, Grazia M.S. Mancini, Jorge L. Juncos, Pirayeh Eftekhari, Nataliya Di Donato, Marjolijn C.J. Jongmans, Laurence Faivre, Gilles Morin, Małgorzata J.M. Nowaczyk, Didier Lacombe, Zeichi-Seide Roseli, Conny M. A. van Ravenswaaij, Daniela Melis, Julien Masliah-Planchon, William B. Dobyns, Alexander Hoischen, Hatice Koçak Eker, Marlies Kempers, Andreas Rump, Vera Uliana, Victoria Mok Siu, Fabienne Giuliano, Nicole Philip, Beate Albrecht, Omar A Abdul-Raman, Alain Verloes, Mirjam Klaus, Angela E. Lin, Massimiliano Rossi, Albert David, Bregje W.M. van Bon, Jeanette C. Ramer, Ludivine Templin, Séverine Drunat, Yves Sznajer, Vincent Procaccio, Jean-Baptiste Rivière, Mary Ella M Pierpont, Francesca Faravelli, Judith Allanson, Leina Guion Almeida, Daniela T. Pilz, Cristina Rusu, Nicolas Chassaing, Charles Marques Lourenço, Bruce H. Wainer, Valérie Drouin-Garraud
Publikováno v:
European Journal of Human Genetics, 23(3), 292. Nature Publishing Group
Eur J Hum Genet
Eur J Hum Genet, 2014, 23, pp.292-301. ⟨10.1038/ejhg.2014.95⟩
European Journal of Human Genetics, 23(3), 292-301. Nature Publishing Group
European Journal of Human Genetics, 23, 3, pp. 292-301
European Journal of Human Genetics, 23, 292-301
European Journal of Human Genetics, Vol. 23, no.3, p. 292-301 (2014)
Paediatrics Publications
Eur J Hum Genet
Eur J Hum Genet, 2014, 23, pp.292-301. ⟨10.1038/ejhg.2014.95⟩
European Journal of Human Genetics, 23(3), 292-301. Nature Publishing Group
European Journal of Human Genetics, 23, 3, pp. 292-301
European Journal of Human Genetics, 23, 292-301
European Journal of Human Genetics, Vol. 23, no.3, p. 292-301 (2014)
Paediatrics Publications
International audience; Baraitser-Winter, Fryns-Aftimos and cerebrofrontofacial syndrome types 1 and 3 have recently been associated with heterozygous gain-of-function mutations in one of the two ubiquitous cytoplasmic actin-encoding genes ACTB and A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d59a289fd417971e5c5cbc83f908234
https://dspace.library.uu.nl/handle/1874/335851
https://dspace.library.uu.nl/handle/1874/335851
Autor:
Hampson A. Sisler
Publikováno v:
Orbit. 15:1-8
Downward bowing and/or subluxation of the lower eyelid for reasons of paresis, tissue redundancy, or downward and outward push from behind and above (as in the shallow orbits of Crouzon's or trisomy 21 patients) but not from cicatrization is addresse
Publikováno v:
Orbit (Amsterdam, Netherlands). 27(1)
Spontaneous globe luxation is a rare and distressing phenomenon. We report three cases which characterise the aetiology of spontaneous anterior globe luxation in the presence of a shallow orbital configuration and lax eyelids. All patients suffered f