Foveal Hypoplasia in Patients with Stickler Syndrome-Reference-Cited by-同舟云学术

Foveal Hypoplasia in Patients with Stickler Syndrome

Published:2017-06 Issue:6 Volume:124 Page:896-902
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Matsushita Itsuka^ORCID,Nagata Tatsuo,Hayashi Takaaki^ORCID,Kimoto Kenichi,Kubota Toshiaki^ORCID,Ohji Masahito,Kusaka Shunji^ORCID,Kondo Hiroyuki

Publisher

Elsevier BV

Subject

Ophthalmology

Reference26 articles.

1. Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix;Richards;Am J Hum Genet,2000

2. Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 gene;Donoso;Surv Ophthalmol,2003

3. Prevention of retinal detachment in Stickler syndrome: the Cambridge prophylactic cryotherapy protocol;Fincham;Ophthalmology,2014

4. Giant premacular bursa: a novel finding of the posterior vitreous in two patients with Stickler syndrome type 1 revealed by swept-source optical coherence tomography;Chen;Graefes Arch Clin Exp Ophthalmol,2015

5. Maturation of the human fovea: correlation of spectral-domain optical coherence tomography findings with histology;Vajzovic;Am J Ophthalmol,2012

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