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Ophthalmic Genetics Volume 38, 2017 - Issue 6
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Case Reports

Retinal capillaritis in a CRB1-associated retinal dystrophy

Vittoria MurroDepartment of Translational Surgery and Medicine, Eye Clinic, University of Florence, Florence, Italy
,
Dario Pasquale MuccioloDepartment of Translational Surgery and Medicine, Eye Clinic, University of Florence, Florence, ItalyCorrespondence[email protected]
,
Andrea SodiDepartment of Translational Surgery and Medicine, Eye Clinic, University of Florence, Florence, Italy
,
Lorenzo VannozziDepartment of Translational Surgery and Medicine, Eye Clinic, University of Florence, Florence, Italy
,
Cinzia De LiberoOphthalmology Unit, Department of Pediatrics, Anna Meyer Children’s University Hospital, Florence, Italy
,
Gabriele SimoniniRheumatology Unit, NEUROFARBA Department—Pediatric Section, Anna Meyer Children’s Hospital, Florence, Italy
&
Stanislao RizzoDepartment of Translational Surgery and Medicine, Eye Clinic, University of Florence, Florence, Italy
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Pages 555-558 | Received 14 Jul 2016, Accepted 08 Jan 2017, Published online: 27 Jan 2017

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Dario Pasquale Mucciolo, Vittoria Murro, Dario Giorgio, Ilaria Passerini, Andrea Sodi, Gianni Virgili & Stanislao Rizzo. (2018) Long-term follow-up of a CRB1-associated maculopathy. Ophthalmic Genetics 39:4, pages 522-525.
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Articles from other publishers (12)

Xuan-Thanh-An Nguyen, Lude Moekotte, Astrid S. Plomp, Arthur A. Bergen, Maria M. van Genderen & Camiel J. F. Boon. (2023) Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies. International Journal of Molecular Sciences 24:8, pages 7481.
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Malena Daich Varela, Michalis Georgiou, Yahya Alswaiti, Jamil Kabbani, Kaoru Fujinami, Yu Fujinami-Yokokawa, Shaheeni Khoda, Omar A. Mahroo, Anthony G. Robson, Andrew R. Webster, Alaa AlTalbishi & Michel Michaelides. (2023) CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History. American Journal of Ophthalmology 246, pages 107-121.
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Jia-Xing Sun, Hong-Xiang Yan, Dan Hu, Jian Zhou, Yu-Sheng Wang, Jing Wu, Xiao-Jin Song & Xu Hou. (2022) Biallelic Heterozygous Mutations in Crumbs Homolog-1 Gene Associated With Macular Retinoschisis and Angle-Closure Glaucoma: A Case Report and Literature Review. Frontiers in Ophthalmology 2.
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Angela S. Li, Malini Veerappan Pasricha, Kapil Mishra, Quan D. Nguyen, Shannon J. Beres & Edward H. Wood. (2022) CRB1-associated retinal dystrophy presenting as self-resolving opsoclonus and posterior uveitis. American Journal of Ophthalmology Case Reports 26, pages 101444.
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Janet L. Davis. 2022. Albert and Jakobiec's Principles and Practice of Ophthalmology. Albert and Jakobiec's Principles and Practice of Ophthalmology 4161 4191 .
Elli A. Park, Rachel M. Huckfeldt, Jason I. Comander & Lucia Sobrin. (2020) Peripheral Leakage on Ultra-Widefield Fluorescein Angiography in Patients With Inherited Retinal Degeneration. Journal of VitreoRetinal Diseases 5:2, pages 147-156.
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Mays Talib & Camiel J.F. Boon. (2020) Retinal Dystrophies and the Road to Treatment: Clinical Requirements and Considerations. Asia-Pacific Journal of Ophthalmology 9:3, pages 159-179.
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Yalan Zhou, Yutong Jing, Shengru Mao, Jian Liu, Zekai Cui, Yini Wang, Juan Chen, Hon fai Chan, Shibo Tang & Jiansu Chen. (2020) Establishment of induced pluripotent stem cell line CSUASOi004-A by reprogramming peripheral blood mononuclear cells of a PRPF6-related dominant retinitis pigmentosa patient. Stem Cell Research 45, pages 101793.
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Yalan Zhou, Chengcheng Ding, Shutao Xia, Yutong Jing, Shengru Mao, Jian Liu, Juan Chen, Hon fai Chan, Shibo Tang & Jiansu Chen. (2020) Establishment of induced pluripotent stem cell line CSUASOi003- A from an autosomal recessive retinitis pigmentosa patient carrying compound heterozygous mutations in CRB1 gene. Stem Cell Research 44, pages 101742.
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Janet L. Davis. 2020. Albert and Jakobiec's Principles and Practice of Ophthalmology. Albert and Jakobiec's Principles and Practice of Ophthalmology 1 32 .
Vittoria Murro, Dario Pasquale Mucciolo, Andrea Sodi, Ilaria Passerini, Dario Giorgio, Gianni Virgili & Stanislao Rizzo. (2018) Novel clinical findings in autosomal recessive NR2E3-related retinal dystrophy. Graefe's Archive for Clinical and Experimental Ophthalmology 257:1, pages 9-22.
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Sanne K. Verbakel, Ramon A.C. van Huet, Camiel J.F. Boon, Anneke I. den Hollander, Rob W.J. Collin, Caroline C.W. Klaver, Carel B. Hoyng, Ronald Roepman & B. Jeroen Klevering. (2018) Non-syndromic retinitis pigmentosa. Progress in Retinal and Eye Research 66, pages 157-186.
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