Novel ophthalmological features in hereditary endotheliopathy with retinopathy, nephropathy and stroke syndrome

Clinical and Experimental Ophthalmology

Volumn 33, Issue 2, 2005, Pages 181-183

  Cohn, Amy C ^a   Kotschet, Katya ^b   Veitch, Alistair ^b   Delatycki, Martin B ^c   McCombe, Mark F ^a  

^a ROYAL VICTORIAN EYE AND EAR HOSPITAL   (Australia)

^b MONASH MEDICAL CENTRE   (Australia)

^c MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

Author keywords

Endotheliopathy; Nephropathy; Retinopathy; Stroke; Vasculopathy

Indexed keywords

ADULT; ARTICLE; AUSTRALIA; CASE REPORT; CHROMOSOME 3P; CHROMOSOME MAP; FEMALE; GENE IDENTIFICATION; GENE LOCUS; HUMAN; KIDNEY DISEASE; LEUKOENCEPHALOPATHY; LINKAGE ANALYSIS; PEDIGREE; PHENOTYPE; RETINOPATHY; STROKE; VASCULAR DISEASE;

ADULT; CEREBROVASCULAR ACCIDENT; CHROMOSOMES, HUMAN, PAIR 3; ENDOTHELIUM, VASCULAR; FEMALE; FLUORESCEIN ANGIOGRAPHY; HUMANS; KIDNEY DISEASES; LINKAGE (GENETICS); PEDIGREE; RETINAL DISEASES; RETINAL VESSELS; SYNDROME;

EID: 18644369123     PISSN: 14426404     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1442-9071.2005.00976.x     Document Type: Article

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