Cataract development in Norwegian patients with congenital aniridia

Author:

Edén Ulla1,Lagali Neil1,Dellby Anette1,Utheim Tor P.23,Riise Ruth4,Chen Xiangjun5,Fagerholm Per1

Affiliation:

1. Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden

2. Department of Medical Biochemistry, Oslo University Hospital, Oslo, Norway

3. Schepens Eye Research Institute, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts, USA

4. Department of Ophthalmology, Innland Hospital, Elverum, Norway

5. Synslaser Kirurgi AS, Oslo, Norway

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Reference9 articles.

1. PAX6 aniridia and interhemispheric brain anomalies;Abouzeid H;Mol Vis,2009

2. Pathologic Epithelial and Anterior Corneal Nerve Morphology in Early-Stage Congenital Aniridic Keratopathy

3. A NovelPAX6Mutation in Chinese Patients with Severe Congenital Aniridia

4. A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family;Jin C;Mol Vis,2012

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1. An uncommon presentation of WAGR syndrome with persistent fetal vasculature;Journal of American Association for Pediatric Ophthalmology and Strabismus;2023-12

2. New horizons in aniridia management: Clinical insights and therapeutic advances;Taiwan Journal of Ophthalmology;2023

3. Clinical and molecular aspects of congenital aniridia – A review of current concepts;Indian Journal of Ophthalmology;2022

4. Congenital aniridia – A comprehensive review of clinical features and therapeutic approaches;Survey of Ophthalmology;2021-11

5. Crystalline lens alterations in congenital aniridia;Archivos de la Sociedad Española de Oftalmología (English Edition);2021-11

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