Mnemonics
Below is a list of helpful mnemonics and classic clinical triads to aid resident ophthalmologists in preparing for OKAPs and Board exams
Cornea
Principal Corneal Stromal dystrophies, abnormality and staining - "Marylin Monroe Always Gets Her Men in L. A. County"
- Macular dystrophy - Mucopolysaccharide - Alcian blue
- Granular dystrophy - Hyaline materials - Masson trichrome
- Lattice dystrophy - Amyloid - Congo red
BIG is LARGE: BIGH3gene defect in
- Lattice
- Avellino
- Reis-Buckler's
- Granular
- Empty
Gelatinous Mac & CHED-AR: Autosomal recessive (AR) corneal dystrophies
- Gelatinous drop-like
- Macular
- CHED
Keratoconus Ocular Findings - "CONES"
- Central Scarring & Fleischer Ring
- Oil Drop Reflex / edema (hydrops)
- Nerves prominent
- Excessive bulging of lower lid on down gaze (Munson’s Sign)
- Striae (Vogt’s)
Tearing and Excessive Lacrimation - "FACE"
- Foreign Body or Corneal Abrasions
- Acute glaucoma
- Conjunctivitis
- Emotion
Drugs that Cause Cataract - "ABCD"
- Amiodarone
- Busulfan
- Chlorpromazine
- Dexamethasone
Glaucoma
Anterior angle structures (posterior to anterior) - “I Can’t See This Stuff"
- Iris
- Ciliary body
- Scleral spur
- Trabecular meshwork
- Schwalbe's line
Secondary Glaucoma - "NIPPLES T "
- Neovascular
- Iridoschisis
- PXF
- Pigmentary
- Lens (phacolytic/phacomorphic)
- Iridocorneal Endothelial Syndromes
- Seclusio Pupillae (in iritis)
- Trauma (angle recession)
Pediatrics
Congenital corneal opacity/clouding - "STUMPED"
- Sclerocornea
- Tears in Descemets (trauma)
- Ulcer
- Mucopolysaccharidosis/Metabolic
- Peter's anomaly
- Edema: Congenital hereditary endothelial dystrophy (CHED)
- Dermoid
Congenital toxoplasmosis (Sabin’s Triad) - Triad
- Hydrocephalus
- Intracranial calcifications
- Chorioretinitis
Congenital syphilis (Hutchinson’s triad) - Triad
- Interstitial keratitis
- CN VIII deafness
- Hutchinson teeth
Duane’s retraction syndrome subtypes - Count the "Ds"
- Type 1: abDuction affected
- Type 2: aDDuction affected
- Type 3: abDuction and aDDuction affected
Leukocoria - "nPRREDICCCTIV"
- Norrie disease
- Persistent fetal vasculature
- Retinoblastoma
- Retinopathy of prematurity
- Endophthalmitis
- Dysplasia of retina
- Inflammatory cycliticmembrane
- Congential cataract
- Coats disease
- Coloboma of choroid or optic disc
- Toxocariasis
- Incontinentia pigmenti
- Vitreal- Familial Exudative Vitreoretinopathy
Retina
Angioid streak etiology - “PEPSI HAM”
- Pseudoxanthoma Elasticum
Ehlers-Danlos(note this is a famous myth! ) [1][2][3]- Paget's disease of bone
- Sickle cell anemia or other hemoglobinopathy (Thalassemias)
- Idiopathic
- Homocysteinuria
- Acromegaly
- Marfans syndrome
Susac syndrome - Triad
- Encephalopathy
- Hearing loss
- Retinal artery branch occlusions ("boxcar” segmentation)
Acute retinal necrosis - Triad
- Occlusive retinal arteriolitis
- Vitritis
- Multifocal yellow-white peripheral retinitis
Presumed ocular histoplasmosis syndrome - Triad
- Multiple white, atrophic choroidal scars (punched out) = “histo spots"
- Peripapillary pigment changes
- CNV (causing maculopathy and no vitreous cells)
Cherry Red Spot - "Cherry Trees Never Grow Tall"
- Central retinal artery occlusion
- Tay-Sachs disease
- Niemann-Pick Disease
- Gaucher’s disease
- Trauma (Berlin’s Edema)
Neuro-ophthalmology/Uveitis
Leber's hereditary optic neuropathy - Triad
- Hyperemia and elevation of disc (although disc is swollen it does not leak)
- Peripapillary telangiectasia
- Tortuosity of medium sized retinal arterioles
Optic nerve sheath meningioma - Triad
- Painless, slowly progressive vision loss
- Optic atrophy
- Optociliary shunt vessels
Miller-Fisher syndrome - Tetrad
- Facial diplegia
- ophthalmoplegia
- Ataxia
- Areflexia
Granulomatosis with polyangiitis (formerly Wegener’s) - Triad
- Necrotizing granulomatous vasculitis of upper and lower respiratory tract
- Focal segmental glomerulonephritis
- Necrotizing vasculitis of small arteries and veins
Argyll Robertson Reflex - ARP
- ARP acronym left to right is A(ccomodation) R(eflex) P(resent)
- ARP acronym right to left is P(upil) R(eflex) A(bsent)
Prisms A-Null nystagmus: Prism Apex towards Null point to decrease head turn
Oculoplastics
Blepharophimosis - Triad
- Ptosis
- Epicanthus inversus
- Telecanthus
Nerves passing through the Superior Orbital Fissure - "Live Free To See No Insult at All"
- Lacrimal Nerve (CN V1)
- Frontal Nerve (CN V1)
- Trochlear Nerve (CN IV)
Superior Division of Oculomotor Nerve (CN III)
- Nasociliary Nerve (Branch of CN V1)
- Inferior Division of Oculomotor Nerve (CN III)
- Abducens Nerve (CN VI)
Structures passing through the Annulus of Zinn: 3 'n 3 = 6
- CN 3 superior branch
- Nasociliary nerve
- CN 3 inferior branch
- CN 6
Structures passing above the Annulus of Zinn: LOFT
- Lacrimal nerve (CN V1)
- Ophthalmic vein (superior)
- Facial nerve (CN V)
- Trochlear nerve (CN IV)
Orbital wall bones
- Medial wall - SMELL (nearest to nose)
- Sphenoid, Maxilla, Ethmoid, Lacrimal, Lesser wing (Sphenoid)
- Floor - Z's in the PM on the floor
- Zygomatic, Palatine, Maxilla
- Lateral wall - oh GeeZe
- Greater wing of Sphenoid, Zygomatic
- Roof - Frontless
- Frontal, Lesser wing of Sphenoid
Ocular Oncology
Ocular Melanoma high risk features versus nevus
1) "To Find Small Ocular Melanoma Doing IMaging"
Note: "TFSOM- Using Helpful Hints Daily" was superseded by the above. [4]
- Thickness - >2mm
- Fluid - Subretinal fluid
- Symptoms
- Orange pigment
- Melanoma hollow on ultrasound
- DIaMeter > 5 mm on fundus photography
2) MOLES [5]
- Mushroom shape
- Orange pigment
- Large size (>2mm thickness, > 5mm diameter)
- Enlarging tumor
- Subretinal fluid
Miscellaneous
Causes of Ectopia Lentis - "Watch Him See"
- Weill-Marchesani
- Aniridia
- Trauma
- Congenital Glaucoma
- Hyperlysinemia
- Homocystinuria
- Iris coloboma
- Marfan syndrome
- Sulfite oxidase deficiency
- Ehlers Danlos Syndrome
- Ectopia lentis et pupillae
References
- ↑ Singman et al.. Angioid Streaks Are Not a Common Feature of Ehlers-Danlos Syndrome. JAMA Ophthalmol. 2019;137(3):239
- ↑ Mahroo OA, Hykin PG. Confirmation That Angioid Streaks Are Not Common in Ehlers-Danlos Syndrome. JAMA Ophthalmol. 2019 Dec 1;137(12):1463. doi: 10.1001/jamaophthalmol.2019.2549. PMID: 31556922.
- ↑ Perez-Roustit S, Nguyen DT, Xerri O, Robert MP, De Vergnes N, Mincheva Z, Benistan K, Bremond-Gignac D. Manifestations ophtalmologiques des syndromes d’Ehlers–Danlos : à propos d’une cohorte de 21 patients [Ocular manifestations in Ehlers-Danlos Syndromes: Clinical study of 21 patients]. J Fr Ophtalmol. 2019 Sep;42(7):722-729. French. doi: 10.1016/j.jfo.2019.01.005. Epub 2019 May 25. PMID: 31133401.
- ↑ Retina. 39(10):1840-1851
- ↑ Cancers.2020, 12(5), 1311