Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Macular scar"'
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-4 (2019)
Abstract Background Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II) is a rare disease that is assumed to be caused by a pericentrin (PCNT) gene mutation. Clinical manifestations have been reported in pediatrics and neurology; how
Externí odkaz:
https://doaj.org/article/456254a6d0464230bad6ee97644107ed
Akademický článek
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Akademický článek
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Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 59, Iss 2, Pp 208-209 (2021)
Retinal hemangioblastoma is a rare benign retinal vascular tumor that occurs sporadically or in association with von Hippel-Lindau (VHL) disease. If associated with VHL, it can be multiple and/or bilateral. All retinal hemangioblastoma cases should b
Externí odkaz:
https://doaj.org/article/631002bbddec4eb3ae90e2226b3703ae
Akademický článek
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Publikováno v:
Optometry and Vision Science. 98:109-112
Significance Alagille syndrome is rare genetic disease, which affects liver and heart function. Cases are frequently diagnosed late, and a complete ocular examination aids in the diagnosis. Although ophthalmic manifestations are usually benign, occas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b91315f7b66286cb5662dae666538f29
https://doi.org/10.1097/opx.0000000000001641
https://doi.org/10.1097/opx.0000000000001641
Autor:
Sophia El Hamichi, Abdelbarre Oubaaz
Publikováno v:
The Pan African Medical Journal, Vol 24, Iss 325 (2016)
A 8 years old girl suffers from strabismus since her first months of life. Her visual acuity was very low and could only see fingers moving in her left eye. Her left eye fundus showed a chorioretinal scar in the macula due to congenital toxoplasmosis
Externí odkaz:
https://doaj.org/article/72bc77d330964cf991e65ecaaee14164
Publikováno v:
American Journal of Ophthalmology. 214:9-13
Purpose Congenital macular lesions attributed to toxoplasmosis may limit potential visual acuity. The appearance and location of these scars may cause physicians to overlook associated amblyopia. This study reviews the visual outcomes and benefits of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e75b21b7b3a1acb6ba64c0a3e8a4b87
https://doi.org/10.1016/j.ajo.2020.01.034
https://doi.org/10.1016/j.ajo.2020.01.034
Autor:
E. Martín García, J.J. Chávarri García, B. Jiménez del Rio, S.M. Guallar Leza, L. Rodríguez Vicente, J.L. del Río Mayor
Publikováno v:
Archivos de la Sociedad Española de Oftalmología (English Edition). 95:90-93
A 12-year-old patient diagnosed with congenital toxoplasmosis, with no systemic treatment at the time, who presented with a decreased visual acuity (VA) in his left eye (LE). On examination, VA in the LE was 0.05 and the fundus examination revealed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88b152584e74f343e344afb7b995cd47
https://doi.org/10.1016/j.oftale.2019.11.002
https://doi.org/10.1016/j.oftale.2019.11.002
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-4 (2019)
BMC Pediatrics
BMC Pediatrics
Background Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II) is a rare disease that is assumed to be caused by a pericentrin (PCNT) gene mutation. Clinical manifestations have been reported in pediatrics and neurology; however, onl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff43879b0efa217a38eb17b30f63d64c
http://link.springer.com/article/10.1186/s12887-019-1685-2
http://link.springer.com/article/10.1186/s12887-019-1685-2