| Literature DB >> 21158358 |
Enzo Maria Vingolo1, Serena Salvatore, Pier Luigi Grenga, Pietro Maffei, Gabriella Milan, Jan Marshall.
Abstract
Alström syndrome is a multisystemic disorder characterized by cone-rod dystrophy, hearing loss, obesity, insulin resistance and hyperinsulinemia, type 2 diabetes mellitus, dilated cardiomyopathy, and progressive hepatic and renal dysfunction. The cone-rod retinal dystrophy usually develops within a few weeks after birth. The authors examined a young boy with Alström syndrome by means of microperimetry and spectral domain optical coherence tomography (OCT). Instead of the typical alterations observed in cone-rod dystrophies, the characteristics of the central foveal tissue suggest signs of retinal immaturity, with only a single layer of short, thick cones and rods and immature short outer segments. High-speed and high-resolution spectral domain OCT allowed a detailed analysis of retinal layers in a young patient with Alström syndrome for the first time. Copyright 2010, SLACK Incorporated.Entities:
Mesh:
Year: 2010 PMID: 21158358 PMCID: PMC3015152 DOI: 10.3928/01913913-20100507-05
Source DB: PubMed Journal: J Pediatr Ophthalmol Strabismus ISSN: 0191-3913 Impact factor: 1.402