Doyne honeycomb retinal dystrophy – functional improvement following subthreshold nanopulse laser treatment: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s13256-018-1935-1.pdf
Reference18 articles.
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3. Stone EM, et al. A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy. Nat Genet. 1999;22:199–202.
4. Gregory CY, et al. The gene responsible for autosomal dominant Doyne’s honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16. Hum Mol Genet. 1996;5:1055–9.
5. Souied EH, et al. Optical coherent tomography features of malattia leventinese. Am J Ophthalmol. 2006;141:404–7.
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