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Juvenile Macular Degenerations.

Authors :
Altschwager P
Ambrosio L
Swanson EA
Moskowitz A
Fulton AB
Source :
Seminars in pediatric neurology [Semin Pediatr Neurol] 2017 May; Vol. 24 (2), pp. 104-109. Date of Electronic Publication: 2017 May 23.
Publication Year :
2017

Abstract

In this article, we review the following 3 common juvenile macular degenerations: Stargardt disease, X-linked retinoschisis, and Best vitelliform macular dystrophy. These are inherited disorders that typically present during childhood, when vision is still developing. They are sufficiently common that they should be included in the differential diagnosis of visual loss in pediatric patients. Diagnosis is secured by a combination of clinical findings, optical coherence tomography imaging, and genetic testing. Early diagnosis promotes optimal management. Although there is currently no definitive cure for these conditions, therapeutic modalities under investigation include pharmacologic treatment, gene therapy, and stem cell transplantation.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1558-0776
Volume :
24
Issue :
2
Database :
MEDLINE
Journal :
Seminars in pediatric neurology
Publication Type :
Academic Journal
Accession number :
28941524
Full Text :
https://doi.org/10.1016/j.spen.2017.05.005