Low Vision Rehabilitation of a Stargardt-Like Macular Dystrophy Linked to a Novel ELOVL4 Heterozygous Mutation in a Hispanic Family.
Background: Stargardt disease (STGD), the most common juvenile form of macular degeneration, is typically autosomal recessive, inherited from an ABCA4 gene mutation. With advancements in genetic testing, novel potentially pathogenic variants have been phenotypically linked to STGD. We will discuss t...
| Publicado en: | Optometry & Visual Performance Vol. 10; no. 2; pp. 109 - 122 |
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| Autores principales: | , , , |
| Formato: | case study diagnostic images pictorial tables/charts Journal Article |
| Publicado: |
Optometric Extension Program
Jun2022
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| Acceso en línea: | Ver este registro en EBSCOhost |