| Literature DB >> 32587203 |
Rodrigo Clemente-Tomas1, Noemí Ruíz-Del Río1, Amparo Gargallo-Benedicto1, Francisca García-Ibor1, José M Hervas-Hernándis1, Antonio M Duch-Samper2.
Abstract
A 13-year-old child diagnosed with neurofibromatosis type 1 who on a routine control presented with rhegmatogenous retinal detachment associated to dialysis of the ora serrata in the left eye (OS). There were no clinical signs or history of contuse ocular trauma. Neurofibromatosis produces alterations in fibroblasts of the cortex of the vitreous base. This results in deficient production of the collagen fibers that anchor the vitreous base to the pars plana and the peripheral neurosensory retina. Thus, suboptimal function of the fibroblasts explains spontaneous avulsion of the vitreous base. Such avulsion in turn is related to dialysis of the ora serrata.Entities:
Keywords: Dialysis of the ora serrata; fibroblasts; neurofibromatosis type 1; rhegmatogenous retinal detachment; vitreous base
Mesh:
Year: 2020 PMID: 32587203 PMCID: PMC7574055 DOI: 10.4103/ijo.IJO_1895_19
Source DB: PubMed Journal: Indian J Ophthalmol ISSN: 0301-4738 Impact factor: 1.848