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Optical coherence tomography detects retinal changes in hereditary cerebral amyloid angiopathy
Author(s) -
Etten E. S.,
Boer I.,
Steenmeijer S.R.,
AlNofal M.,
Wermer M. J. H.,
Notting I. C.,
Terwindt G. M.
Publication year - 2020
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/ene.14507
Subject(s) - medicine , retinal , nerve fiber layer , interquartile range , cerebral amyloid angiopathy , cohort , ophthalmology , optical coherence tomography , leber's hereditary optic neuropathy , atrophy , retina , pathology , gastroenterology , optic neuropathy , cardiology , optic nerve , disease , neuroscience , dementia , biology
Dutch‐type hereditary cerebral amyloid angiopathy (CAA) mutation carriers showed thinning of the retinal nerve fiber layer compared with controls using spectral domain optical coherence tomography. Retinal fiber layer thinning may be a candidate marker of disease in hereditary CAA.