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Black diaphragm aniridia intraocular lens for aniridia and albinism
Graefe's Archive for Clinical and Experimental Ophthalmology, 2004Our aim was to assess the safety and efficacy of primary and secondary implantation of a black diaphragm aniridia intraocular lens (IOL) in patients that lacked a complete iris diaphragm.This was a retrospective non-comparative study of six eyes in five patients with iris defects.
Victoria W Y, Wong +3 more
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Acta Ophthalmologica Scandinavica, 2007
Abstract Purpose: Our purpose was to analyze the various ocular manifestations, treatment options, and the possible outcome of congenital aniridia (CA) a rare and severe developmental disorder. Methods: 52 eyes of 26 patients were regularly checked with full eye examination including anterior segment photography.
M POPPER +5 more
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Abstract Purpose: Our purpose was to analyze the various ocular manifestations, treatment options, and the possible outcome of congenital aniridia (CA) a rare and severe developmental disorder. Methods: 52 eyes of 26 patients were regularly checked with full eye examination including anterior segment photography.
M POPPER +5 more
openaire +1 more source
The Indian Journal of Pediatrics, 2003
Aniridia (absence of iris) is a congenital, bilateral, uncommon panocular disorder. Whereas the occurrence of aniridia in the general population is 1:50000, it is present in about 1 in 70 patients with Wilm's tumor. This aniridia is sporadic and Wilm's tumor in these cases presents at an unusually early age.
Manisha, Nada +3 more
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Aniridia (absence of iris) is a congenital, bilateral, uncommon panocular disorder. Whereas the occurrence of aniridia in the general population is 1:50000, it is present in about 1 in 70 patients with Wilm's tumor. This aniridia is sporadic and Wilm's tumor in these cases presents at an unusually early age.
Manisha, Nada +3 more
openaire +2 more sources
Aniridia-Wilms’ Tumour Syndrome
Ophthalmologica, 1977The association of aniridia and Wilms' tumour constitutes a real syndrome, which is genetic. It may either be autosomal dominant or depend on a chromosomal deletion or also, according to Knudson's theory, be due to two mutational events, the initiating mutation being germinal and the promoting mutation being post-zygotical.
J, François, D, Coucke, R, Coppieters
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Congenital aniridia – A comprehensive review of clinical features and therapeutic approaches
Survey of Ophthalmology, 2021Erlend Christoffer Sommer Landsend +2 more
exaly
Pathophysiology of aniridia-associated keratopathy: Developmental aspects and unanswered questions
Ocular Surface, 2021Daniel Aberdam
exaly