| Literature DB >> 27463631 |
Ana Filipa Miranda1, Maria Daniela Rivera-Monge1, Charles Costa Farias1,2.
Abstract
Rothmund-Thomson syndrome (RTS) is a rare dermatosis with about 300 cases reported to date. The authors describe two siblings with RTS and inflammatory conjunctival disease featuring fornix shortening and symblepharon as well as palpebral disease with sparse eyelashes. These cases demonstrate RTS ocular surface findings different to those usually described.Entities:
Mesh:
Year: 2016 PMID: 27463631 DOI: 10.5935/0004-2749.20160053
Source DB: PubMed Journal: Arq Bras Oftalmol ISSN: 0004-2749 Impact factor: 0.872