Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism-Reference-Cited by-同舟云学术

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Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism

Published:2021-02-17 Issue:3 Volume:42 Page:243-251
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Ehrenberg Miriam¹²^ORCID,Bagdonite-Bejarano Laura³,Fulton Anne B.³,Orenstein Naama²⁴,Yahalom Claudia⁵

Affiliation:

1. Ophthalmology Unit, Schneider Children’s Medical Center in Israel, Petach Tikva, Israel

2. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

3. Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts, USA

4. Genetic Department, Children’s Medical Center in Israel, Petach Tikva, Israel

5. Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2021.1888128

Reference28 articles.

1. Foveal hypoplasia and optical coherence tomographic imaging

2. The clinical evaluation of infantile nystagmus: What to do first and why

3. The Size of the Foveal Avascular Zone Is Associated with Foveal Thickness and Structure in Premature Children

4. Foveal abnormalities determined by optical coherence tomography angiography in children with history of retinopathy of prematurity

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1. Novel pathogenic variants of SLC38A8 gene and literature review;European Journal of Ophthalmology;2024-03-22

2. Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci;Nature Communications;2024-02-21

3. Foveal Hypoplasia in a Child With Tyrosinase-Positive Albinism;Cureus;2023-09-02

4. Best-corrected visual acuity results facilitate molecular diagnosis of infantile nystagmus patients harboring FRMD7 mutations;Experimental Eye Research;2023-08

5. Multi-omics analysis in human retina uncovers ultraconservedcis-regulatory elements at rare eye disease loci;2023-06-12

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