Retina and Optic nerve Flashcards
primary vitreous
secondary vitreous
tertiary vitreous
- primary: vessels of hyaloid, macrophages, collagenous fibrillar material, mesenchymal cells
- seconday: primitive hyalocytes, hyaluronic acid, and monocytes. Persists in adults as formed vitrous
- tertiary: secreted by ciliary epithelium and becomes lens zonules + vitreous base
persistant hyaloid artery
usually not a problem
- mittendorf’s dot: attached to posterior lens capsule
- bergmeister’s papilla: large remnant on optic disc
persistent hyperplastic primary vitreous
- most commonly with Dobermans and Staffordshire
- “white pupil” is a common sign
- most frequent problems are spontaneous hemorrhage and cataract
asteroid hyalosis
Ca or lipid deposition in the vitreous
not considered a problem
mostly older animals
what are the 10 layers of the retina
- RPE (retinal pigmented epithelium)
- photoreceptors
- external limiting membrane
- outer nuclear layer (nuclei of rods and cones)
- outer plexiform layer (synaptic layer for photoreceptors, bipolar cells, and horizontal cells)
- inner nuclear layer (nuclei of bipolar, horizontal, amacrine and muller cells)
- inner plexiform layer (synaptic layer for bipolar and amacrine cells)
- ganglion cell layer
- nerve fiber layer(connected to optic nerve)
- internal limiting membrane
what are the 4 retinal vascular patterns
- holangiotic (dog, cat, cattle, sheep, pig)
- paurangiotic (horse)
- merangiotic (rabbit)
- anangiotic (birds and reptiles)
collie eye anomaly (CEA)
- autosomal recessive with no sex or coat predisposition
- only progressive if coloboma is present
- phenotypic signs include: coloboma (hole in an eye structure) , choroidal hypoplasia, retinal detachment, retinal hemorrhage
what is progressive retinal atrophy
- autosomal recessive
- always bilateral
- can do genetic testing
- no treatment
- electroretinography testing at 1.5-2yrs old
progressive retinal atrophy clinical signs
- rods go first, so lose night vision first
- decreased PLR so tapetal is hyperreflective
- attenuated vessels
- pale optic disc
- cataract formation
- should have some detectable ERG activity but no SARD activity
CPRA (central progressive retinal atrophy) or RPED (retinal pigment epithelial dystrophy)
- usually only seen in England
- day blindness
retinal dysplasia
- abnormal formation of retina (from small folds to complete detachment)
- usually present at birth with no progression
- autosomal recessive (cocker, lab, springer spaniel, bedlington, sealyham)
- can be secondary to infectious dz (FeLV, BVD, adenovirus)
merle ocular dysgenesis
associated with marling gene
wide range of abnormalities
-homozygous: multiple ocular defects, predominantly white
-heterozygous: occasional ocular defects
SARD (sudden acquired retinal degeneration)
- sudden complete blindness
- usually middle aged overweight females
- may be associated to Cushing’s
- no known treatment
- no ERG activity, if there is ANY then diagnosis needs to correlate with brain or optic nerve
FCRD (feline central retinal degeneration)
often incidental finding
associated with Taurine deficiency
progression from grade 1-5
______ is associated with acute blindness in cats
enrofloxacin (baytril)
-more associated with parenteral administration