Results 151 to 160 of about 19,020 (198)

Epidemiology of aniridia in Sweden and Norway

open access: yesActa 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

open access: yesOcular 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
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Aniridia

International Ophthalmology Clinics, 2008
Stacey C, Brauner   +2 more
  +6 more sources

Aniridia and wilm’s tumor

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
openaire   +2 more sources

Keratopathy in Congenital Aniridia

The Ocular Surface, 2003
Although the most apparent clinical finding in aniridia is the absence of iris tissue, additional ocular structures are often affected. Mutations of the Pax 6 gene, which is important for eye development, have been identified in families with members affected by aniridia.
Kristine L, Mayer   +3 more
openaire   +2 more sources

Aniridia: A Comparative Overview

American Orthoptic Journal, 2014
Aniridia is linked to a mutation of the PAX6 gene, which results in panocular anomalies. A set of common secondary pathologies associated with aniridia is recognized. Much of the literature on aniridia focuses on genetic factors of the disorder and associated abnormalities, both ocular and nonocular. The field of research on the prevalence of pathology
Paula, Schanilec, Ronald, Biernacki
openaire   +2 more sources

Corneal Changes in Aniridia

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
openaire   +2 more sources

Aniridia and congenital ptosis

Plastic and Reconstructive Surgery, 1975
Congential ptosis associated with aniridia was found in 3 patients from 2 pedigrees. Nonsurgical aphakia, a condition not previously reported in association with aniridia, was also found in one case. The association of aniridia and congenital ptosis is suggested as evidence for the common mesodermal etiology of both anomalies.
M B, Shields, J W, Reed
openaire   +2 more sources

Cataract surgery and aniridia

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

A Family Study of Aniridia

Archives of Ophthalmology, 1961
Introduction In June of 1959, the Canadian National Institute for the Blind requested the Blindness Control Division of the Canadian Department of National Health and Welfare to investigate the unusual number of cases of blindness due to aniridia in several families living in a circumscribed rural area in Eastern Canada.
J H, GROVE, M W, SHAW, G, BOURQUE
openaire   +2 more sources

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