Literature DB >> 2090400

Familial vascular retinopathy. A preliminary report.

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.

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Year:  1990        PMID: 2090400     DOI: 10.1007/BF00164839

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  2 in total

1.  Cerebroretinal vasculopathy. A new hereditary syndrome.

Authors:  M G Grand; J Kaine; K Fulling; J Atkinson; S B Dowton; M Farber; J Craver; K Rice
Journal:  Ophthalmology       Date:  1988-05       Impact factor: 12.079

2.  Retinal and choroidal ischemic syndrome, digestive tract and renal small vessel hyalinosis, intracerebral calcifications and phenotypic abnormalities: a new family syndrome.

Authors:  G van Effenterre; J Haut; A Brezin; Y Le Mer; J C Rambaud; A Galian; G Touchard; E Rothschild
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1989       Impact factor: 3.117

  2 in total
  2 in total

Review 1.  Genetic factors in cerebral small vessel disease and their impact on stroke and dementia.

Authors:  Christof Haffner; Rainer Malik; Martin Dichgans
Journal:  J Cereb Blood Flow Metab       Date:  2016-01       Impact factor: 6.200

Review 2.  New roles for the major human 3'-5' exonuclease TREX1 in human disease.

Authors:  David Kavanagh; Dirk Spitzer; Parul H Kothari; Aisha Shaikh; M Kathryn Liszewski; Anna Richards; John P Atkinson
Journal:  Cell Cycle       Date:  2008-06-16       Impact factor: 4.534

  2 in total

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