Abstract | BACKGROUND: METHODS: A retrospective chart review was performed in individuals with retinal degeneration and two likely disease-causing variants in RDH12. RESULTS: 57 subjects were enrolled from nine countries. 33 subjects had clinical records available from childhood. The data revealed an EOSRD, with average age of onset of 4.1 years. Macular atrophy was a universal clinical finding in all subjects, as young as 2 years of age. Scotopic and photopic electroretinography (ERG) responses were markedly reduced in all subjects, and a non-recordable ERG was documented as young as 1 year of age. Assessment of visual acuity, visual field and optical coherence tomography revealed severe loss of function and structure in the majority of subjects after the age of 10 years. Widefield imaging in 23 subjects revealed a unique, variegated watercolour-like pattern of atrophy in 13 subjects and sparing of the peripapillary area in 18 subjects. CONCLUSIONS: This study includes the largest collection of phenotypic data from children with RDH12-associated EOSRD and provides a comprehensive description of the timeline of vision loss in this severe, early-onset condition. These findings will help identify patients with RDH12-associated retinal degeneration and will inform future design of therapeutic trials.
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Authors | Abigail T Fahim, Zaina Bouzia, Kari H Branham, Neruban Kumaran, Mauricio E Vargas, Kecia L Feathers, N Dayanthi Perera, Kelly Young, Naheed W Khan, John R Heckenlively, Andrew R Webster, Mark E Pennesi, Robin R Ali, Debra A Thompson, Michel Michaelides |
Journal | The British journal of ophthalmology
(Br J Ophthalmol)
Vol. 103
Issue 12
Pg. 1789-1796
(12 2019)
ISSN: 1468-2079 [Electronic] England |
PMID | 30979730
(Publication Type: Journal Article, Multicenter Study, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | © Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. |
Chemical References |
- Alcohol Oxidoreductases
- RDH12 protein, human
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Topics |
- Adolescent
- Adult
- Age of Onset
- Aged
- Alcohol Oxidoreductases
(genetics)
- Child
- Child, Preschool
- Color Vision
(physiology)
- DNA Mutational Analysis
- Electroretinography
- Eye Diseases, Hereditary
(diagnosis, genetics, physiopathology)
- Female
- Genotype
- Humans
- Male
- Middle Aged
- Mutation
- Night Vision
(physiology)
- Phenotype
- Retina
(physiopathology)
- Retinal Dystrophies
(diagnosis, genetics, physiopathology)
- Retrospective Studies
- Tomography, Optical Coherence
- Visual Acuity
(physiology)
- Visual Fields
(physiology)
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