| Literature DB >> 8796162 |
E Bonnar1, P Logan, P Eustace.
Abstract
A patient with a 20 year history of severe keratoconjunctivitis of unknown origin was found, on assessment at a blepharitis clinic, to have complete absence of meibomian glands. Further examination revealed the features of EEC syndrome. To our knowledge, this is the only case to have been diagnosed in this way. The ocular complications of EEC syndrome and other ectodermal dysplasias are reviewed.Entities:
Mesh:
Year: 1996 PMID: 8796162 DOI: 10.1038/eye.1996.73
Source DB: PubMed Journal: Eye (Lond) ISSN: 0950-222X Impact factor: 3.775