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Ocular manifestations of equine motor neuron disease
Author(s) -
RIIS R. C.,
JACKSON C.,
REBHUN W.,
KATZ M. L.,
LOEW E.,
SUMMERS B.,
CUMMINGS J.,
LAHUNTA A.,
DIVERS T.,
MOHAMMED H.
Publication year - 1999
Publication title -
equine veterinary journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.82
H-Index - 87
eISSN - 2042-3306
pISSN - 0425-1644
DOI - 10.1111/j.2042-3306.1999.tb03801.x
Subject(s) - pathognomonic , lipofuscin , retinal , batten disease , horse , pathology , retinal degeneration , retina , fundus (uterus) , motor neuron , biology , medicine , ophthalmology , anatomy , disease , neuroscience , paleontology
Summary The characteristics of the ocular manifestations of equine motor neuron disease (EMND) are described. Forty‐two horses with histories, clinical signs and necropsies compatible with EMND were the subjects of this study. Ophthalmoscopic lesions that varied in severity were found in 40 of 42 horses and appeared as a distinct pigmented reticulated pattern at the tapetal‐nontapetal junction or throughout the fundus, depending upon severity. The pattern colours ranged from yellow brown to black. Areas of hyperreflectivity formed mosaic patterns in the tapetal fundus. ERG B‐wave amplitudes were usually at least 50% reduced and many animals showed extinguished amplitudes. None of the horses had apparent visual impairment. Histopathologically, all 42 horses had retinal pigment epithelial (RPE) congestion with ceroid‐lipofuscin. Retinal degeneration was variable even within the eyes. Thin layer chromatography (TLC) analysis of the RPE and neural retina identified both green and orange emitting fluorescent compounds not found in normal horses. All unsupplemented horses had plasma vitamin E levels <1.0 μg/ml. The potential significance of this report is the pathognomonic role the ocular manifestations exhibit in helping to diagnose equine motor neuron disease. In memory of John Cummings, we dedicate this manuscript.