Retinal features in Mulvihill-Smith syndrome.

CONCLUSIONS: This is the first report of retinal features in Mulvihill-Smith syndrome. These ocular changes coincided with other systemic changes with the onset of adulthood. These changes may indicate the natural history of retinal features in this progeria syndrome with short life span. The detailed analysis and progression of structural changes in retina is possible with optical coherence tomography. PMID: 27268268 [PubMed - as supplied by publisher]

http://www.ncbi.nlm.nih.gov/pubmed/27268268?dopt=Abstract

Source: Ophthalmic Genetics - June 9, 2016 Category: Opthalmology Tags: Ophthalmic Genet Source Type: research