Resolution of cystoid macular edema with topical carbonic anhydrase inhibitor in a patient with retinal dystrophy associated with Cohen syndrome

Author:

Sevik Mehmet Orkun1ORCID,Aykut Aslan1ORCID,Şahin Özlem1ORCID

Affiliation:

1. Department of Ophthalmology, Marmara University School of Medicine, Istanbul, Turkey

Funder

No funding

Publisher

Informa UK Limited

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Reference18 articles.

1. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies

2. Wang H, Falk MJ, Wensel C, Traboulsi EI. Cohen syndrome. GeneReviews. [Internet] Initial posting. 2006 Aug 29; Last update 2016 Jul 21.

3. The human gene mutation database. [Internet] [accessed 2020 Aug 15]. http://www.hgmd.cf.ac.uk/ac/gene.php?gene=VPS13B.

4. The ophthalmic findings in Cohen syndrome

5. Ophthalmologic findings in cohen syndrome

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