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Ophthalmic Genetics Volume 37, 2016 - Issue 4
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Case Reports

Intraretinal cystoid spaces in a patient with retinitis pigmentosa due to mutation in the MAK gene

Yu-Hung LaiPediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital, Philadelphia, Pennsylvania, USA;Department of Ophthalmology, Kaohsiung Medical University Hospital, and Department of Ophthalmology, School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, TaiwanView further author information
,
Jenina E. CapassoPediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital, Philadelphia, Pennsylvania, USAView further author information
,
Richard KaiserRetina Service, Wills Eye Hospital, Philadelphia, Pennsylvania, USAView further author information
&
Alex V. LevinPediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital, Philadelphia, Pennsylvania, USA;Thomas Jefferson University, Philadelphia, Pennsylvania, USACorrespondence[email protected]
View further author information
Pages 424-426 | Received 13 May 2015, Accepted 05 Sep 2015, Published online: 19 Feb 2016

Citations (7)

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Read on this site (3)

Yuhong Gan, Xiongze Zhang, Ling Chen & Feng Wen. (2020) Intraretinal Cystoid Spaces in Regression of Punctate Inner Choroidopathy Lesions. Ocular Immunology and Inflammation 28:6, pages 938-946.
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T. A. C. de Guimaraes, J. E. Capasso & A. V. Levin. (2019) Paradoxical response to carbonic anhydrase inhibitors in patients with intraretinal cystoid spaces. Ophthalmic Genetics 40:3, pages 213-218.
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Joanna Monika Gray, Harry Otway Orlans, Morag Shanks, Penny Clouston & Robert Elvis MacLaren. (2018) Slowly progressive retinitis pigmentosa caused by two novel mutations in the MAK gene. Ophthalmic Genetics 39:4, pages 508-511.
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Articles from other publishers (4)

Masood Naseripour, Sara Hemmati, Samira Chaibakhsh, Arzhang Gordiz, Leila Miri & Fatemeh Abdi. (2022) Cystoid macular oedema without leakage in fluorescein angiography: a literature review. Eye 37:8, pages 1519-1526.
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Young Ju Lew, Nicholas Rinella, Jia Qin, Joanna Chiang, Anthony T. Moore, Travis C. Porco, Austin Roorda & Jacque L. Duncan. (2018) High-resolution Imaging in Male Germ Cell–Associated Kinase (MAK)-related Retinal Degeneration. American Journal of Ophthalmology 185, pages 32-42.
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Chiara M. Eandi, Laura Dallorto, Roberta Spinetta, Maria Pia Micieli, Mario Vanzetti, Alessandro Mariottini, Ilaria Passerini, Francesca Torricelli, Camilla Alovisi & Cristiana Marchese. (2017) Targeted next generation sequencing in Italian patients with Usher syndrome: phenotype-genotype correlations. Scientific Reports 7:1.
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Yu-Hung Lai & Kwou-Yeung Wu. (2017) Ocular genetics in Taiwan. Current Opinion in Ophthalmology 28:5, pages 430-435.
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