Paradoxical response to carbonic anhydrase inhibitors in patients with intraretinal cystoid spaces
Author:
Affiliation:
1. Pediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital, Philadelphia, Pennsylvania, USA
2. Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA
Funder
The Foerderer Fund (AVL) and the Robison D. Harley, MD Endowed Chair in Pediatric Ophthalmology and Ocular Genetics
Robison D. Harley, MD Endowed Chair in Pediatric Ophthalmology and Ocular Genetics
Publisher
Informa UK Limited
Subject
Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/13816810.2019.1622021
Reference40 articles.
1. Retinal Dystrophy with Intraretinal Cystoid Spaces Associated with Mutations in the Crumbs Homologue (CRB1) Gene
2. Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK gene
3. Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations
4. Autosomal Recessive Bestrophinopathy
5. Macular cysts in retinal dystrophy
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