Pupillary Disorders Flashcards
Hypoplastic iris
Assoc w/ cataracts, glaucoma, macular/ON hypoplasia
Aniridia
AR
Bilaterally displaced pupil (inf-temp), lens in oppo direction
Microspherophakia, miosis, poor dilation
Assoc: severe axial myopia, RD, large K, cataract, transillumination
Ectopia lentis et papillae
Inherited as isolated finding
Idiopathic tractional = fibrous tethers margin to peripheral K
Ectopic pupil
Inf/inf-nasal notch
Assoc: chorioretinal/ON
Cause: isolation/idiopathic, chromosomal, congenital
Coloboma
Spoke-like opacities across pupil
From tunica vasculosa lentis
Persistent pupillary membrane
AC cleaveage anomalies
-Peters vs Riegers
P = central
R = peripheral
Corneal defects
RAPD
- main cause
- appearance
- assoc
Optic tract lesion = contralateral
Amaurotic pupil
Vision loss
Upgaze paresis, head tilt
Contralateral APD
Light-near dissociation
Pretectal pupil - Parinaud syndrome/dorsal MB
Pretectal pupil
-where damage is that causes light-near dissociation
Efferent/PNS pathway:
EW -> inf CN3 -> ciliary g. -> sphincter (miosis) & ciliary (accomm)
Poor direct, normal consensual
Light-near dissociation
Miosis in darkness
Argyll-robertson
Argyll-robertson
- location of lesion
- causes
Fibers b/w pretectal and PNS nucleus
DM, alcohol, neurosyphilis
CN3 palsy
- CN3 and PNS fibers
- when suspect aneurysm
PNS are superficial to CN3 = susceptible to compression
CN3 + dilated pupil
Poor light response
Loss of accommodation
Decr corneal sensitivity
Tonic pupil
Tonic pupil
- lesion location
- gtt
Ciliary g. or short ciliary n.
1% pilo = constriction
Idiopathic, women 20-40
Significant miosis with 0.125% pilo
Adie’s