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Ophthalmic Genetics Volume 35, 2014 - Issue 2
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Case Reports

Falciform Macular Folds and Chromosome 22q11.2: Evidence in Support of a Locus for Familial Exudative Vitreoretinopathy (FEVR)

Jarel K. GandhiDepartment of Ophthalmology and Vision Science
,
Travis T. TollefsonDepartment of Otolaryngology-Head and Neck Surgery, University of California, Davis Medical Center Sacramento, CAUSA
&
David G. TelanderDepartment of Ophthalmology and Vision ScienceCorrespondence[email protected]
Pages 112-116 | Received 17 Jun 2012, Accepted 17 Feb 2013, Published online: 22 Mar 2013

Citations (4)

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Read on this site (1)

Dongmei Qi, Sha Liu & Tao Yu. (2020) Characterization of Unique Lens Morphology in a Cohort of Children with Familial Exudative Vitreoretinopathy. Current Eye Research 45:10, pages 1222-1227.
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Articles from other publishers (3)

Noemí Güemes-Villahoz, Dhariana Acón, Sophia El Hamichi, Rebecca Tanenbaum & Audina M. Berrocal. (2021) Serpiginous Intraretinal Lesions Associated With Familial Exudative Vitreoretinopathy. Ophthalmic Surgery, Lasers and Imaging Retina 52:3, pages 155-159.
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Hamid-Reza Moein, Hajirah N. Saeed, Deborah S. Jacobs, Yuna Rapoport, Michael K. Yoon, Ankoor S. Shah, Haumith Khan, Duna Raoof & Ula V. Jurkunas. (2019) Exposure, entropion, and bilateral corneal ulceration in a newborn as a manifestation of chromosome 22 q11.2 duplication syndrome. American Journal of Ophthalmology Case Reports 13, pages 16-19.
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Rui Zhang, Xin Sun & Bo Niu. (2017) The importance of pegaptanib sodium treatment for patients with vascular active vitreoretinopathy. Experimental and Therapeutic Medicine.
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