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101 Cards in this Set

  • Front
  • Back
Ddx Salt and Pepper Fundus
(6)
Rubella
Lebers Congenital Amaurosis
Carriers (albinism, choroideremia, retinitis pigmentosa)
CPEO
Cystinosis
Drug toxixity
Ddx of Bull’s Eye Retinopathy
(8)
Cone dystrophy (most common)
Chloroquine/hydroxychloroquine
Stargardt’s
Speilmeyer-Vogt-Batten-Mayou
AMD
Neimann-Pick (type B)
North Carolina Dystrophy
Benign Concentric Annular Dystrophy
Ddx CME
(8)
N- nicotinic acid
E- epinephrine
V- venous occlusion
E- prostaglandin E2
R- Retinitis pigmentosa

D- DM
I- Irvine-Gass
P- pars planitis, parafoveal telangiectasia
Ddx of Decreased Vision with Normal Fundus
(6)
Stargardt’s
Cone dystrophy
CSCR
CME
Twig BRVO/BRAO
Toxic retinopathy
Order of Severity in Proliferative Sickle Cell Retinopathy
(4)
SC > Sthal > SS > SA
Risk Factor for CRVO
(8)
HTN
POAG
PACG
Atherosclerosis
DM
PCV
Collagen vascular disease
Dysprotinemia
What do Macroaneurysms do?
(4)
R- rupture
A- artery occlusion
F- fluid
T- thrombose
Risk Factors for AMD
(9)
Age
Hyperopia
Family Hx
Smoking
Hyperlipidemia
Complement factor H
Soft drusen
Pigment clumping
PED
Ddx of Retinal Crystals
(8)
Tamoxifen (occur in NFL and IPL)
Canthaxanthine
Oxalosis
Bietti syndrome
Autosomal dominant crystalline dystrophy
Calcified macular drusen
Talc
Methoxyflurane (leads to Calcium oxalate)
Ddx for Cherry Red Spot
(4)
Tay-Sach
Neimann-Pick
Sandhoff
CRAO
Ddx Foveal Hypoplasia
(3)
Aniridia
Albinism
PHPV
Ddx Accommodative ET
(11)
Pseudo ET
Nystagmus blockade
Duanes syndrome
Mobius syndrome
6th nerve palsy
Neurologic disorders
Sensory deprivation
Cyclic ET
Acquired non-accommodative ET
Divergence insufficiency
Divergence paralysis (think pontine tumors or head trauma)
Ddx Brown’s Syndrome
(5)
Inferior oblique palsy
Double elevator syndrome
(if no restriction do KNAPP procedure = move MR and LR to SR)
Blowout fracture
Thyroid disease
Ddx Lens Dislocation
(8)
Marfan’s
Homocystinuria
Weill-Marchesani syndrome
Hyperlyseinemia
Sulfite Ox
Ehler-Danlos syndrome
Syphilis
PXE
Ddx Optic Nerve Hypoplasia
(8)
Aniridia
Drugs (LSD, PCP, Dilantin, Cocaine, Quinine)
ETOH
Maternal DM
Aicardi syndrome
DeMorsier’s syndrome
Young maternal age
Trisomy 18 and 21
Ddx Drugs that cause optic nerve hypoplasia
(5)
LSD
PCP
Dilantin
Cocaine
Quinine
Ddx Craniofacial Syndromes
(3)
Goldenhar syndrome
Waardenberg syndrome
Pierre-Robin syndrome
Ddx Craniosynostosis Syndrome (Autosomal Dominant and give V Patterns)
(3)
Couzon syndrome
Apert syndrome
Pfeiffer syndrome
Ddx Heterochromia Iridis
(4)
Congenital horner’s syndrome
Fuch’s
Waardenberg
Siderosis
Increases Risk of ET
(4)
Caucasian
Smoking
Increased maternal age
Low birth weight
Increases Risk of XT
(2)
Smoking
Low birth weight
Hyphema in Children
(8)
JXG
Trauma
ROP
PHPV
Coat’s
Retinoblastoma
Leukemia
Bleeding abnormalities
Ddx Paradoxical Pupil Response
(4)
Congenital stationary night blindness
Achromatopsia
Optic nerve hypolpasia
Leber's Congenital Amaurosis
Ddx Spasmus Nutans
(2)
Chiasmal glioma (given “bowtie” atrophy of the nerve)
Necrotizing encephalomyopathy
Ddx Optic Nerve Drusen (75-86% Bilateral)
(5)
PXE
Retinitis pigmentosa
Angioid streaks
Chorioretinal folds
Migranes
Risk Factors for NAION
(8)
HTN
DM
Smoking
Hyperlipidemia
Migraine
Vasculitis
Chronic renal failure
Dialysis
Lebers Hereditary Optic Neuropathy
(2)
11778 is the most common
14484 is the most likely to spontaneously improve
Ddx Optociliary Shunt Vessels
(7)
Optic nerve meningioma
Sphenoid wing meningioma
Optic nerve glioma
CRVO
Chronic papilledema
Arachnoid cyst of the optic nerve
Glaucoma
Ddx Toxic Retinopathy
(12)
Ethambutol
INH
Chloramphenicol
Hydroxyquinolones
Penicillamine
Cisplatin
Vincristine
Methanol
Ethelene glycol
Etoh
Digitalis
Amiodarone
Ddx Downbeat Nystagmus (Located at the Cervico-Medullary Junction) (Treat with Clonazepam and Baclofen)
(7)
Arnold-chiari
Tumor
Demyelination
CVA
Meds (ETOH, Li, anti-seizure meds)
Wernickes
Platybasia
Ddx Monocular Nystagmus
(4)
Chiasmal glioma
Hypothalamus glioma
MS
Spasmus nutans
Ddx Upbeat Nystagmus (Located in the Posterior Fossa)
(4)
Demyelination
CVA
Cerebellar degeneration
Tobacco
Ddx See-Saw Nystagmus
(3)
Craniopharyngioma
Parasellar tumor
Trauma
Demographics and Etiology for Parinaud’s “Dorsal midbrain syndrome”
(3)
Young men = pineal tumor
Women = MS
Old men = CVA
Ddx Light-Near Dissociation
(7)
Argyll-Robertson (bilateral)
Dorsal midbrain (bilateral)
Adie’s (unilateral or bilateral)
Optic neuropathy
Severe retinal disease
Aberent regeneration of CN III
S/p PRP
Ddx of Things that Increase in Pregnancy (9)
CSCR
HTN retinopathy/DM retinopathy
Purtscher-like retinopathy
Retinal detachment
TTP
CRVO/CRAO
BRVO/BRAO
Ischemic optic neuropathy
CC fistula
Ddx Papilledema
(4)
Mass
Hydrocephalus
Meningitis
Pseudotumor
Ddx Things that Pregnancy Aggrevate
(7)
Uveal melanoma
Pituitary adenoma
Meningioma
Hemangioma
DM
Graves disease
Fibrous dysplasia
Ddx Meds that Aggrevate Myasthenia Gravis
(5)
Beta-blockers
Clindamycin
D-penicillamine
Anti-seizure meds
Lidocaine
Ddx “fat” EOMs
(4)
Graves disease (tendons spared)
Pseudotumor (tendons involved)
Metastasis (prostate)
Acromegaly
Ddx Double Elevator Syndrome
(5)
Congenital usually presents with ptosis
Trauma
Graves
MG
Supranuclear cause
Ddx Congenital Nystagmus
(5)
Albinism
Aniridia
Achromatopsia
Atrophic/hypoplastic optic nerve
Lebers congenital amaurosis
Ddx Canalicular Obtruction
(9)
5-FU
Docetaxol
Idoxuridine
Phospholine iodine
Eserine
Vaccinia
HSV
Pemphagoid
Stevens Johnson syndrome
Ddx Dacrolyths
(3)
Actinomyces
Candida
Epinephrine
Ddx Bright Things on T1 MRI
(4)
Subacute blood
Melanin
Lipid
Mucous
Ddx Well-Circumscribed Orbital Tumor
(8)
Cavernous hemangioma
Fibrous hystiocytoma
Schwanomma
Neuofibroma
Hemangiopericytoma
Dermoid cyst
Pleomorphic adenoma
Lymphoma
Ddx Poorly-Circumscribe Orbital Tumor
(6)
Pseudotumor
Lymphangioma
Hemorrhage
Cellulitis
Sarcoid
Wegeners
Ddx Variable Appearance of Orbital Tumors
(4)
Rhabdomyosarcoma
Metastasis
Lymphoproliferative disorders
Adenoid cystic carcinoma
Ddx of High Internal Reflectivity
(4)
Lymphangioma
Pseudotumor
Cavernous hemangioma
Neurofibroma
Ddx Retained Lens Nuclei
(3)
Rubella
Lowe’s syndrome
Trisomy 13
Risk Factors for POAG
(5)
Increased IOP
Increased age
Decreased CCT
Race
Positive family history
Risk Factors for PACG
(4)
Family history
Female
55-65yo
Hyperope
Ddx Splinter Hemorrhage
(5)
Glaucoma
PVD
DM
BRVO
Anticoagulation
Risk Factors for Normal Tension Glaucoma (5)
Migraines
Reynauld’s syndrome
Ischemic vascular disease
Autoimmune disorder
Japanese
Risk Factors for Bleb-Associated Endophthalmitis
(10)
Blepharitis
Conjunctivitis
Trauma
NLD obstruction
Contact lens use
Bleb leak
Male
Young
Inferior limbal bleb
5-FU/MMC
Ddx Secondary Glaucoma with Uveitis
(6)
HSV
VZV
Sarcoid
Posner schlossman
Fuchs
UGH
Ddx of Increased Risk of Steroid Responder
(6)
POAG
<10yo
Relative with POAG
DM
High myope
Connective tissue disease
Ddx Pseudo-Glaucomatous Cups
(4)
Chiasmal compression (bowtie atrophy)
AAION
Toxic (methanol)
Hypotension
Risk Factors for Choroidals after Glaucoma Surgery
(4)
Aphakia/pseudophakia
Myopia
Prior PPV
Pre-op IOP > 30
Ddx for ACUTE Follicles
(4)
Adenovirus
HSV
Acute hemorrhagic conjunctivitis
Newcastles
Ddx CHRONIC Follicles
(4)
Chlamydia
Meds (atropine, epinephrine, trifluridine)
Molluscum
Lymphoma
Ddx for Type-I Hypersensitivity Reaction (AB-Mediated)
(4)
Vernal keratoconjunctivitis
Atopic keratoconjunctivitis
Allergic conjunctivitis
Hay fever
Ddx for Type-II Hypersensitivity Reaction (Cytotoxic AB)
(4)
OCP
VKH
Sympathetic ophthalmia
Mooren’s ulcer
Ddx for Type-III Hypersensitivity Reaction (Immune Complex/Complement Cascade)
(5)
Steven-Johnson syndrome
Peripheral staph marginal keratitis
Scleritis
PUK
Phacoanaphylaxis
Ddx Type-IV Hypersensitivity Reaction (T-cell Mediated)
(7)
Vernal keratoconjunctivitis
Phlyctenulosis (associated with staph and TB)
Staph blepharitis
Contact dermatitis
Granulomatous response to TB and Sarcoid
Acne rosacea
Corneal graft rejection
Ddx of Parinaud’s Oculoglandular Syndrome
(11)
Cat scratch (Bartonella)
TB
Syphilis
Sporotrichosis
Tularemia
Mono
Leptothrix
Rickettsia
Chlamydia
Sarcoid
Actinomyces
Who gets Nevus of Ota
(5)
Asians
Blacks
Duanes
Retinitis pigmentosa
Congenital cataracts
Ddx of Bacterial Corneal Ulcer
(5)
Staph
Step
Pseudomonas
Moraxella
Serratia
Ddx of Things that Perforate Intact Epithelium
(6)
N. meningiditis
N. Gonococcus
Shigella
Corynbacteremia diphtheriae
Listeria
Haemophilis aegypsia
Ddx Interstitial Keratitis
(8)
Syphilis
Lyme
EBV
Cogan’s (also deaf)
HSV
HZO
Sarcoid
Acanthamoeba
Ddx Anterior Scleritis
(8)
Syphilis
Lyme
TB
HZO
Sarcoid
Gout
Leprosy
Immune disease
Ddx of Congenital Cloudy Cornea
(7)
S- sclerocornea
T- tears in descemet’s
U- ulcer (infections)
M- metabolic (mucopolysaccharidosis)
P- peter’s
E- edema (CHED and PPMD)
D- dermoids
Ddx of Corneal Dystrophies with BIGH3 Gene (Chrom 5)
(4)
Reis-Buckler
(type I with rods)
(type II with “curly” filaments and known as Theil-Behnke)
Granular
Avellino
Lattice type I
Ddx Corneal Crystals
(10)
Schnyder’s
Multiple myeloma
Lipid keratopathy
Gout
Infectious crystalline keratopathy (strep viridans)
Bietti syndrome
Cystinosis
Tryosinemia
Plant soaps (dieffenbachia)
Clofizimine
Things Associated with Keratoconus
(13)
Downs
Lebers congenital amaurosis
Ehlers-Danlos
Connective tissue disorder
Vernal keratoconjunctivitis
Aniridia
Retinitis pigmentosa
Atopic keratoconjunctivitis
Marfans
Hard contact lens
Eye rubbing
Floppy eyelid syndrome
Floppy mitral valve syndrome
Things Associated with Keratoglobus
(3)
Lebers congenital amaurosis
Connective tissue disease
Ehler-Danlos (type IV)
Things that Induce Stevens-Johnson Syndrome
(5)
Sulfa
PCN
Barbiturates
Dilantin
Infections (HSV, measles, mycoplasma)
Things that can Induce OCP (Treat with Cellcept, Dapsone, Steroids, Cyclophasphamide)
(4)
Pilocarpine
Phospholine iodine
Timolol
IDU
Ddx of Mucopolysaccarides that cause Cloudy Corneas
(5)
Hurler
Scheie
Matquio
Moroteaux-Lamy
Sly

NOT SANFILLIPO
Ddx Toxic Medicomentosa
(4)
Aminoglycosides
Trifluridine
Proparacaine
Preserved AT’s
Ddx Corneal Verticallata
(5)
Aminodarone
Fabry’s
Chloroquine
Indomethacin
Chlorpromazine
Ddx “true” Membrane
(4)
Diphtheria
GC
Beta-hemolytic strep
Stevens-Johnson’s syndrome
Ddx “pseudo” Membrane
(8)
HSV
EKC
PCF
Staph
Pneumococcus
Pseudomonas
Chemicals
OCP
Ddx Enlarged Corneal Nerves
(6)
MEN-IIb
Phytanic acid (Refsum syndrome)
Leprosy
Riley-Day
Neurofibromatosis type 1
Acanthamoeba
Ddx Prominent Nerves
(5)
Keratoconus
Icthyosis
Fuchs corneal dystrophy
Corneal edema
Congenital glaucoma
Ddx Retinoblastoma
(3)
Toxocariasis
PHPV
Coats
Ddx Conjunctival Telangiectasia
(4)
Osler-Weber-Rendu
Louis Barr
Fabrys
Sturge-Weber
Ddx False Positive VDRL
(4)
SLE
Liver disease
Pregnancy
Other treponemal disease
Ddx Hemorrhage in all Layers of the Retina
(5)
AMD
Macroaneurysm
Valsalva retinopathy
Shaken Baby
Terson's
Ddx Purtscher’s Retinopathy
Trauma
(7)
Acute pancreatitis
Chronic renal failure
Autoimmune disease
Amniotic fluid embolism
Retrobulbar anesthesia
Orbital steroid injection
Ddx of Stellate KP
(5)
HSV
VZV
Sarcoid
Fuchs
Toxoplasmosis
Ddx Uveitis with Hyphema
(8)
HLA-B27 uveitities
HSV
VZV
Post-op endophthalmitis
UGH
Behcet
Fuchs
Traumatic iritis
Ddx with PAX 6 Gene
(3)
Aniridia
Peters
Congenital cataracts
Ddx HLA- B27 Uveitis (Non-Granulomatous)
(5)
Ankylosing spondylitis (90% +)
Reiters (85-95% +)
IBD
Psoriatic
Reactive
Ddx Drug Induced Uveitis
(2)
Rifabutin
Cidofivir
Ddx of Intermediate Uveitis
(7)
Pars planitis
Syphilis
Lyme
Sarcoid
MS
TB
Toxocariasis
Ddx Band Keratopathy
(6)
Chronic ocular disease (JRA)
Hyercalcinemia
hyper PTH, vit D toxicity, sarcoid
Hereditary
Increased serum phosphorus (renal failure)
Mercury vapors
Silicone oil in aphakic patient
Ddx of Neurotrophic Cornea
(7)
HSV
VZV
CVA/aneurysm of CN V nerve body
MS
Leprosy
Hereditary (riley-day syndrome)
Anesthesia abuse
Systemic Diseases Associated with Pediatric Glaucoma
(5)
Sturge-Weber
NF-1 (no glaucoma in NF-2)
Marfan
Homocysteinemia
Weill-Marchesani
Side Effects for CAIs
(5)
Aplastic anemia
Thrombocytopenia
Agranulocytosis
Hypokalemia
Kidney stones
Risk Factors for “Wipe-Out” in Glaucoma Surgery
(3)
Advanced age
Pre-op split fixation
Early hypotony early elevation of IOP