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Ophthalmic Genetics Volume 39, 2018 - Issue 6
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Case Reports

FEVR findings in patients with Loeys-Dietz syndrome type II

Mark A. SolinskiRetinal Consultants, Des Plaines, IL, USAORCID Iconhttp://orcid.org/0000-0002-3659-9639
ORCID Icon,
Michael P. BlairRetinal Consultants, Des Plaines, IL, USA;Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, IL, USA;Department of Ophthalmology and Visual Sciences, University of Chicago, Chicago, IL, USA
,
Harry DietzHoward Hughes Medical Institute and The McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA;Division of Pediatric Cardiology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA;Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA
,
David MittelmanAdvocate Lutheran General Hospital, Park Ridge, IL, USA
&
Michael J. ShapiroRetinal Consultants, Des Plaines, IL, USA;Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, IL, USACorrespondence[email protected]
Pages 754-758 | Received 12 Jun 2018, Accepted 30 Sep 2018, Published online: 08 Nov 2018

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Toshiaki Asano, Kazuma Oku & Hiroyuki Kondo. (2021) Familial exudative vitreoretinopathy with TGFBR2 mutation without signs of Loeys-Dietz syndrome. Ophthalmic Genetics 42:5, pages 637-640.
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Articles from other publishers (5)

Yao Lu & Zhizhong Ma. (2023) Novel pathogenic TGFBR1 variant identified in an adult with acquired retinal arterial macroaneurysm in loeys-dietz syndrome. European Journal of Ophthalmology 33:6, pages NP10-NP13.
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Wenting Wang, Hui Man, Jie Zhang, Penglin Yu, Shuchan Li, Xinyan Xu & Nan Li. (2021) Ocular findings in two Chinese children with Loeys-Dietz syndrome. European Journal of Ophthalmology 32:6, pages NP55-NP59.
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Katherine Loomba, Daniela Lin, Willis Lin & Bernadette Riley. (2022) Ocular Manifestations of Loeys–Dietz Syndrome. EMJ Rheumatology.
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Hiroyuki Kondo, Itsuka Matsushita, Tatsuo Nagata, Etsuko Fujihara, Katsuhiro Hosono, Eiichi Uchio, Yoshihiro Hotta & Shunji Kusaka. (2021) Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene . Translational Vision Science & Technology 10:7, pages 18.
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Dominder Kaur & Bryce A. Kerlin. 2021. Management of Bleeding Patients. Management of Bleeding Patients 201 209 .

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