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Demographics, Prevalence, and Characteristics of Limbal Stem Cell Deficiency in Southern California. [PDF]
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Survey of Ophthalmology, 1984
Aniridia occurs as a phenotypically heterogeneous condition which may be inherited as an autosomal dominant disorder or as part of several systemic syndromes. It has been linked with the loci of chromosomes 1 and 2 and associated with the deletion of the p-13 band of chromosome 11. Aniridia may occur in a highly penetrant form in association with other
L B, Nelson +4 more
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Aniridia occurs as a phenotypically heterogeneous condition which may be inherited as an autosomal dominant disorder or as part of several systemic syndromes. It has been linked with the loci of chromosomes 1 and 2 and associated with the deletion of the p-13 band of chromosome 11. Aniridia may occur in a highly penetrant form in association with other
L B, Nelson +4 more
openaire +4 more sources
Specular Microscopy in Aniridia
Cornea, 1987 Aniridia and the iridocorneal endothelial (ICE) syndromes both are conditions which include abnormalities of the cornea, iris, and progressive iridocorneal adhesions which may result in glaucoma. In order to investigate the similarities between aniridia and the ICE syndromes, we performed specular microscopy of the corneal endothelium in nine patients ...
J S, Weiss +3 more
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Black diaphragm aniridia intraocular lens for aniridia and albinism
Graefe's Archive for Clinical and Experimental Ophthalmology, 2004 Our 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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Journal of Glaucoma, 2002
Aniridia is a congenital developmental anomaly of the eye that usually affects both eyes. The development of the iris, cornea, lens, angle, optic nerve and retina is disturbed. Aniridia is most often a hereditary disease with an autosomal dominant, rarely autosomal recessive inheritance, but sporadic cases are also possible.
D, Liláková +3 more
openaire +4 more sources
Aniridia is a congenital developmental anomaly of the eye that usually affects both eyes. The development of the iris, cornea, lens, angle, optic nerve and retina is disturbed. Aniridia is most often a hereditary disease with an autosomal dominant, rarely autosomal recessive inheritance, but sporadic cases are also possible.
D, Liláková +3 more
openaire +4 more sources
Epidemiology of aniridia in Sweden and Norway
Acta Ophthalmologica, 2008 Purpose: To investigate the epidemiology of aniridia in the populations of Sweden and Norway. Methods: A thorough search for aniridia patients has been performed in Sweden and Norway.
David Iggman, Kristina Tornqvist
exaly +2 more sources
Congenital Aniridia and the Ocular Surface
Ocular Surface, 2016 Aniridia is a congenital pan-ocular disorder caused by haplo-insufficiency of Pax6, a crucial gene for proper development of the eye. Aniridia affects a range of eye structures, including the cornea, iris, anterior chamber angle, lens, and fovea.
Robert Ihnatko +2 more
exaly +2 more sources
Current Opinion in Ophthalmology, 2010
In the past years, several new options have been developed for the surgical management of aniridia in the course of cataract surgery.The lens capsule may be altered - thinned - in aniridia, requiring particular attention in order to avoid complications with possible consequences for the surgical plan.
Irmingard M, Neuhann, Thomas F, Neuhann
openaire +2 more sources
In the past years, several new options have been developed for the surgical management of aniridia in the course of cataract surgery.The lens capsule may be altered - thinned - in aniridia, requiring particular attention in order to avoid complications with possible consequences for the surgical plan.
Irmingard M, Neuhann, Thomas F, Neuhann
openaire +2 more sources
American Journal of Ophthalmology, 1979
Nineteen patients with aniridia and one patient with bilateral iris colobomata from eight families were examined for corneal abnormalities. Thirty-six eyes revealed changes that are consistent with a progressive corneal dystrophy. These changes begin in the corneal periphery in the early years of life and progress to the corneal center with increasing ...
G, Mackman, F S, Brightbill, J M, Optiz
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Nineteen patients with aniridia and one patient with bilateral iris colobomata from eight families were examined for corneal abnormalities. Thirty-six eyes revealed changes that are consistent with a progressive corneal dystrophy. These changes begin in the corneal periphery in the early years of life and progress to the corneal center with increasing ...
G, Mackman, F S, Brightbill, J M, Optiz
openaire +2 more sources