| Literature DB >> 2090400 |
C W Storimans1, J A Oosterhuis, M J van Schooneveld, P J Bos, P D Maaswinkel-Mooy.
Abstract
We describe a new hereditary syndrome with an autosomal dominant mode of inheritance, with vascular retinopathy, migraine and Raynaud's phenomenon as the most striking features. The retinopathy is characterized by tortuosity and variable caliber of the retinal vessels, haemorrhages, telangiectases and both central and peripheral vascular occlusions, leading finally to a proliferative retinopathy.Entities:
Mesh:
Year: 1990 PMID: 2090400 DOI: 10.1007/BF00164839
Source DB: PubMed Journal: Doc Ophthalmol ISSN: 0012-4486 Impact factor: 2.379