Clinical Course of Autosomal Recessive Bestrophinopathy Complicated by Choroidal Neovascularization.

Détails

ID Serval
serval:BIB_774A22252B08
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Titre
Clinical Course of Autosomal Recessive Bestrophinopathy Complicated by Choroidal Neovascularization.
Périodique
Ophthalmic surgery, lasers & imaging retina
Auteur⸱e⸱s
Introini U., Casalino G., Khan K.N., Eandi C., Alovisi C., Michaelides M., Bandello F.
ISSN
2325-8179 (Electronic)
ISSN-L
2325-8160
Statut éditorial
Publié
Date de publication
01/11/2018
Peer-reviewed
Oui
Volume
49
Numéro
11
Pages
888-892
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article
Publication Status: ppublish
Résumé
The authors report the clinical course of two cases of autosomal recessive bestrophinopathy (ARB) complicated by choroidal neovascularization (CNV). One patient presenting with a novel BEST1 mutation (c.658 C>T, p.Gln220*) underwent anti-vascular endothelial growth factor therapy. Response to treatment was documented on optical coherence tomography angiography (OCTA). Despite initial response to treatment, recurrent CNV exudation with progressive subretinal fibrosis was observed. In the second patient, the CNV was not treated and spontaneous regression was observed. This report indicates that the clinical course of CNV in ARB may vary considerably, ranging from spontaneous regression to progressive subretinal fibrosis despite intervention. [Ophthalmic Surg Lasers Imaging Retina. 2018;49:888-892.].
Mots-clé
Bestrophins/genetics, Bestrophins/metabolism, Child, Choroid/blood supply, Choroid/pathology, Choroidal Neovascularization/diagnosis, Choroidal Neovascularization/etiology, Choroidal Neovascularization/physiopathology, DNA/genetics, Electroretinography, Eye Diseases, Hereditary/complications, Eye Diseases, Hereditary/diagnosis, Eye Diseases, Hereditary/genetics, Female, Fluorescein Angiography/methods, Fundus Oculi, Humans, Male, Retinal Diseases/complications, Retinal Diseases/diagnosis, Retinal Diseases/genetics, Tomography, Optical Coherence/methods, Visual Acuity
Pubmed
Web of science
Création de la notice
12/03/2021 19:21
Dernière modification de la notice
26/03/2021 6:35
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