Results 151 to 160 of about 5,544 (177)

[Congenital aniridia in children].

La Revue du praticien, 2019
Congenital aniridia in children. Congenital aniridia is a genetic rare disease that affects the entire eyeball (pan-ocular disease). The disease is characterized by partial or complete absence of iris. Clinical signs in children are essentially photophobia and nystagmus.
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Abnormalities of ERG in congenital aniridia.

Yan ke xue bao = Eye science, 1992
Congenital aniridia is generally associated with nystagmus, corneal pannus, cataract, ectopia lentis, glaucoma, macular hypoplasia, optic nerve hypoplasia and compromised visual function. Many theories have been proposed, including a failure in the development of the neural ectoderm and/or an aberrant development of mesoderm.
L, Wu, Q, Ma, Y, Chen, D Z, Wu, T, Luo
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[Extraocular changes in congenital aniridia].

Ceskoslovenska oftalmologie, 1992
The authors draw attention to possible extraocular changes in children with congenital aniridia. Of 31 investigated patients they were found in 5 children. Among these changes, because of its serious character, Wilms tumour holds the first place; it was found by the authors in two children.
M, Odehnal, B, Brůnová, J, Krásný
openaire   +1 more source

Management of Glaucoma in Congenital Aniridia

2015
Glaucoma in aniridia usually develops during childhood, due to either open- or closed-angle mechanisms. In our study of Aniridia Foundation International (AFI) members, approximately half of the subjects developed glaucoma, with glaucoma diagnosis at average age 13.6 years and median age 8.5 years.
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ANIRIDIA 743.45 (Congenital Aniridia, Hereditary Aniridia)

2008
David Sellers Walton, Garyfallia Katsavounidou   +1 more
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Analysis of Choroidal Thickness in Children with Congenital Aniridia

Current Eye Research, 2020
Hui Chen, Xiaohang Wu, Weirong Chen
exaly  

Upstream ORF frameshift variants in thePAX65ʹUTR cause congenital aniridia

Human Mutation, 2021
Alexandra Filatova, Tatyana A Vasilyeva, Andrey V Marakhonov   +2 more
exaly  

Spectral-domain optical coherence tomography foveal morphology as a prognostic factor for vision performance in congenital aniridia

European Journal of Ophthalmology, 2020

exaly  

Recurrent PAX 6 mutation in a Chinese family with congenital aniridia, progressive cataracts and mental retardation

European Journal of Ophthalmology, 2020
Tao Yang
exaly  

Congenital aniridia.

American journal of ophthalmology, 2003
openaire   +3 more sources