Topical carbonic anhydrase inhibitors in macular edema associated with Alström syndrome
Author:
Affiliation:
1. Pediatric Ophthalmology Department, Hospital Universitario La Paz, Madrid, Spain
2. Ophthalmology Department, Hospital Clínico San Borja Arriarán, Santiago, Chile
Publisher
Informa UK Limited
Subject
Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.3109/13816810.2015.1094493
Reference19 articles.
1. Alstrom Syndrome: Genetics and Clinical Overview
2. Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity
3. EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome
4. The Alstrom syndrome: ophthalmic histopathology and retinal ultrastructure.
5. Full-Field Electroretinography and Marked Variability in Clinical Phenotype of Alström Syndrome
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1. Alström syndrome: Two clinical cases with two novel pathogenic variants;European Journal of Ophthalmology;2022-09-13
2. Carbonic Anhydrase Inhibitors in Ophthalmology: Glaucoma and Macular Oedema;Progress in Drug Research;2021
3. Childhood cone–rod dystrophy with macular cyst formation in ABCA4 mutation identified by serial spectral-domain optical coherence tomography;Taiwan Journal of Ophthalmology;2020
4. Carbonic Anhydrase Inhibitor with Topical NSAID Therapy to Manage Cystoid Macular Edema in a Case of Gyrate Atrophy;European Journal of Ophthalmology;2017-08-11
5. Retinitis pigmentosa and bilateral cystoid macular oedema in a patient heterozygous for the RIM1 mutation previously associated with cone-rod dystrophy 7;Ophthalmic Genetics;2016-05-13
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