OPT 313 Inherited Disorders

What is ERG?

CL on the front of the eye measures the mass electrical response of the retina to photopic stimulation

What do the a and b wave show on ERG?

a wave = first negative component = photoreceptors

b wave = bottom of a wave to peak = bipolar and Muller cells

What are the 2 measures we look at on ERG?

amplitude of a and b wave = often reduced in disease

implicit time from flash to wave onset = often increased in disease

What is the purpose of white flash on ERG?

results in a mostly rod response

What is the purpose of colour stimuli on ERG?

cone response

What is the purpose of rapid flicker on ERG?

cone only response since rods cannot follow a fast flicker

What is the purpose of dark-adapted with bright flash on ERG?

mostly a rod response

What is the purpose of light-adapted on ERG?

mostly a cone response

What is the purpose of multifocal testing on ERG?

assesses retinal activity in small areas of retina

What is the purpose of pattern testing on ERG?

assesses ganglion cell activity

What is an EOG?

measures the potential between cornea and Bruch's, specifically at the RPE and mid-retina

Does abnormal ERG and EOG typically occur together in retinal disease?

yes

in Best's disease where there is diffuse RPE atrophy, the ERG may be normal but the EOG is abnormal

What is the dark trough vs light peak seen in EOG?

dark trough = 15min in darkness = depends on integrity of RPE, cornea, lens, CB

light peak = 25min in light = depol of basal RPE membrane

How do we calculate the Arden ratio in EOG?

= light peak / dark trough

What is the lower limit for Arden ratio in normal subjects?

lower limit of 1.8 roughly (below 1.65 is significantly abnormal)

When do we perform genetic testing? 2 situations.

suspected IRD that genes have been identified for

predictive/carrier testing for those who are asymptomatic but have an affected family member (but caution if there is no tx)

What are the 3 reasons we may do genetic testing?

confirm Dx or distinguish between different diseases

improve management with better prognosis, less other testing, more therapies

genetic counseling by identifying inheritance patterns

What are 2 cautions against genetic testing?

do not use to R/O an IRD since not all genes for all diseases are on every panel

discourage testing of adult-onset conditions for minors if there is no available therapy, may worry parents unnecessarily

What is retinitis pigmentosa (RP)?

group of inherited disorders with diffuse progressive bilateral dysfunction of rods, then cones and RPE later (due to PR apoptosis and loss of OS)

What are the main 3 genetic inheritance patterns of RP?

AR in 50-60%

AD in 30-40%

X-linked in 5-15%

NOTE: >100 different genes may cause RP

What is the clinical triad of RP?

artery attenuation due to reduced O2 demand in the retina

bone spicule pigment due to RPE cell migration

waxy ONH pallor

What are some other signs of RP?

vitreous cells

RPE depigmentation/atrophy

What are some symptoms of RP?

night blindeness from rod loss

progressive VF loss from midperiphery to far (ring scotoma!)

reduced contrast

Describe the evolution of RP.

onset based on inheritance pattern = PR loss, then RPE changes = mid-peripheral followed by far-peripheral = central vision affected at end-stage disease

How does RP appear on VF?

isolated scotomas around 20deg from fixation = coalesce into a ring scotoma in midperiphery = expands quickly into far periphery, slowly into central fixation

How does RP appear on EOG?

abnormal BUT note that ERG is typically better test bc more sensitive

How does RP appear on OCT?

cystic macular lesions, ERM, VMT in some RP pt's with reduced central VA - may have outer>inner retinal layer thinning

How does RP appear on FAF?

ring of hyperAF encircles fovea due to increased lipofuscin in RPE (PR degeneration)

hypoAF in periphery due to RPE atrophy

How does RP appear on genetic testing?

RPE65 gene variant (mostly seen in Leber's but some RP also has it)

How does RP appear on ERG?

reduced a and b wave

normal or prolonged implicit time

NOTE: may be undetectable in advanced disease

What are 2 possible complications of RP?

CME

PSC

Which gene specifically is important to note for RP as there is genetic therapy available (esp for young pt's)?

RPE65

What is the tx for RP?

Luxturna gene therapy for RPE65

CAIs for CME - topical or oral

Vit A palmitate in high dosage of 15,000 IU (marginal benefts of 2% slowed progression, lots of risks like liver damage)

retinal prosthesis

LV referral

CAT Sx if PSC develop

What are some benefits of performing CAT Sx in pt's with RP?

visual improvements can include VA, glare, color vision, peripheral vision

better outcomes if better starting VA, more preserved ellipsoid zone on OCT

What are 4 complications of performing CAT Sx in pt's with RP?

zonular weakness in 10-20% of patients

light toxicity = need to decrease to 60% light intensity and cover light when not needed

post-op CME in 10-15% of patients = may need prolonged NSAID, steroid, CAI

PCO in 60-84% of patients = may need YAG

What is RP sine pigmento?

variant of RP = absence of bone-spicule-like pigmentary changes, but still have artery attenuation and atrophy of RPE

What feature of RP sine pigmento is seen here?

perifoveal loss of PR's and RPE on OCT = ring scotoma very close to fixation seen on HVF

What is sectoral RP?

variant of RP = only certain regions show degeneration, but is still symmetrical between eyes

What feature of sectoral RP is seen here?

still has PIL loss and RPE thinning on OCT

What are the 8 main systemic associations seen with RP?

Usher syndrome

Alport syndrome

Kearns-Sayre syndrome

Bardet-Biedl syndrome

Refsum disease

Abetalipoproteinemia

Alstrom disease

Cockayne syndrome

What is Usher syndrome sometimes seen with RP?

AR genetic condition resulting in RP and deafness

What are the 3 main types of Usher syndrome associated with RP?

type 1 = severe hearing & balance loss at birth, nyctalopia by age 10, vision loss later in life

type 2 = hearing loss at birth, nyctalopia by adolescence, vision loss later in life, NORMAL balance

type 3 = progressive hearing loss in childhood, nyctalopia by adolescence, vision loss later in life, NORMAL balance

What is Alport syndrome sometimes seen with RP?

X-linked, AR, or AD genetic condition that affects type IV collagen in early childhood = deafness, RP, kidney disease

Aside from genetic testing, how can we dx Alport syndrome?

kidney biopsy

Aside from deafness, RP, and kidney disease, what other finding of Alport syndrome is seen here?

anterior lenticonus

What is Kearns-Sayre syndrome sometimes seen with RP?

spontaneous or inherited mutation causing impaired ATP production in mitochondria = NM dysfunction by age 20 onset

Aside from genetic testing, how can we dx Kearns-Sayre syndrome?

skeletal mm biopsy will show ragged red fibers due to abnormal mitochondria

CSF test will show protein >1mg/mL, lactate & pyruvate elevated in CSF and blood

What are the 3 main S/S seen in Kearns-Sayre syndrome?

RP or salt-and-pepper fundus

chronic progressive external ophthalmoplegia (CPEO) = progressive paralysis of all EOMs

cardiac abnormalities from conduction deficits

ataxia

dementia

hearing loss

What is Bardet-Biedl syndrome sometimes seen in RP?

AR genetic condition causing ciliopathy throughout the body with juvenile onset

What are some features of Bardet-Biedl syndrome?

rod/cone dystrophy or cone/rod or RP

strabismus

obesity

T2DM

HTN

high Cholesterol

hypogonadism in males

polydactyly

renal anomalies

mental handicap

What is Refsum disease sometimes seen in RP?

AR genetic condition that causes RP vision loss and anosmia

What are some features of Refsum syndrome?

RP vision loss

anosmia = loss of sense of smell

bone abnormalities in hands/feet

progressive mm wasting

poor balance/coordination

hearing loss

dry, scaly skin

cardiac arrhythmias

What is Abetalipoproteinemia sometimes seen in RP?

AR genetic condition that affects fat absorption (intestine) and mobilization (liver) = nutrient deficiency of fat-soluble vitamins like KADE

Aside from genetic testing, how else can we dx Abetalipoproteinemia?

blood work for cholesterol/TAGs/fat-soluble vitamins, acanthocytes

What are some S/S of Abetalipoproteinemia?

progressive neuro deterioration

mm weakness

difficulty walking

liver dysfunction

anemia

cardiac arrhythmia

What is Alstrom syndrome sometimes seen in RP?

AR genetic condition causing ciliopathy throughout the body with onset witihn first 18mos of life

What are the main features of Alstrom syndrome?

cone/rod dystrophy or RP

strabismus

progressive hearing loss

dilated cardiomyopathy

hyperphagia

T2DM

short stature

liver steatosis

kidney failure

acanthosis nigrans

What is Cockayne syndrome sometimes seen in RP?

AR genetic condition that affects genes responsible for DNA repair after UV damage

What are the main features of Cockayne syndrome?

RP-like pigmentary degeneration

skin photosensitivity = burn easily with no increased cancer risk

microcephaly

tooth decay

bone abnormalities

failure to gain weight/grow at expected rate

hearing loss

What is Leber's Congenital Amaurosis?

AR or AD genetic condition inhibits phototransduction

Aside from genetic testing, how can we dx Leber's Congenital Amaurosis?

abnormal ERG (light or dark adapted) = may even be undetectable

What are some ocular signs of Leber's Congenital Amaurosis?

abnormal pupil response

nystagmus

retinal changes may include normal early on, chorioretinal degeneration and atrophy centered around fovea, “bone-spicule" like pigmentation, subretinal flecks, "marbled" fundus, pigmented nummular lesions at RPE level, optic disc abnormalities, “Coats like” reaction

What gene is implicated in some cases of Leber's Congenital Amaurosis?

RPE65

What findings of Leber's Congenital Amaurosis are seen here?

attenuated BV

peripheral pigmentary changes

FAF = peripheral hypopigmented spots and a ring of hyperfluorescence surrounding the fovea

What findings of Leber's Congenital Amaurosis are seen here?

macular atrophic lesion

attenuated BV

peripheral pigmentary changes

What are some symptoms of Leber's Congenital Amaurosis?

photophobia

nyctalopia

profound vision loss 20/200 to NLP even from birth (can progress slowly then stabilize)

What are some signs of Leber's Congenital Amaurosis?

eye rubbing = oculo-digital reflex creates phosphene BUT increased risk for KCN

poor fixation

nystagmus

What is the tx for Leber's Congenital Amaurosis?

Luxturna gene therapy if RPE65

correct Rx

LV referral

What is congenital stationary night blindness?

non-progressive nyctalopia starting from birth

What is the fundus albipunctatus appearance of congenital stationary night blindness?

scattered yellow-white dots in the posterior pole (sparing the macula) that extend to the mid-periphery = dots typically stable, may disappear over time

What is the Oguchi appearance of congenital stationary night blindness?

Mizuo-Nakamura phenomenon = fundus is unremarkable in the dark-adapted state, but has a yellow iridescent (golden) sheen after light exposure

What is the diagnostic testing for congenital stationary night blindness?

scotopic ERG will be abnormal

Aside from the nyctalopia, what are some other ocular findings of congenital stationary night blindness?

reduced VA (20/40 to 20/60)

photophobia

myopia

strabismus

nystagmus

What is the tx for congenital stationary night blindness?

LV referral

high dose 9-cis-beta-carotene may possibly improve VF and ERG results

What is choroideremia?

X-linked dystrophy resulting in progressive degeneration of the RPE, PR's, choriocapillaris = underlying white sclera exposed

What are some features of the appearance of choroidemia?

pigment clumping at the level of the RPE

well-defined atrophy = visible sclera and large choroidal BV remain = mostly in the postequatorial region just outside the arcades; advance centripetally

island of foveal tissue may persist until later stages

What are 2 NORMAL findings seen in choroidemia?

NORMAL appearing retinal BV

NO optic atrophy

What is the evolution of choroidemia?

first decade = nyctalopia

teenage years = peripheral vision loss, good VA maintained

5th-7th decade = rapid VA and color vision loss

What findings of choroidemia are seen here?

scattered pigment clumping

visible large choroidal vessels

fovea = preserved choriocapillaris at the fovea

extrafovea = deficient choriocapillaris and visible medium, large choroidal vessels

What are some diagnostic testing we can perform for choroidemia?

VF = patchy midperipheral irregular scotomas, then near complete loss of central and peripheral vision later on

ERG = abnormal

genetic testing

What are 2 complications of choroidemia?

mac edema

CATs

What is the tx for choroidemia?

LV referral

CAI's or anti-VEGF for mac edema

What is gyrate atrophy?

AR dystrophy that is caused by a deficiency in ornithine aminotransferate (OAT) enzyme = increased ornithine in blood

What are the 3 main findings of gyrate atrophy?

bilateral chorioretinal degeneration in the mid-far periphery = patchy, sharply demarcated circles of atrophy with hyperpigmented margins

early CATs

myopia

How does gyrate atrophy appear on FAF?

hypoAF in the dark margins

hyperAF in the light atrophic areas

What diagnostic testing can we do for gyrate atrophy?

ornithine blood levels

genetic testing

What are some symptoms of gyrate atrophy?

nyctalopia

peripheral VF loss

VA loss

What is the evolution of gyrate atrophy?

first decade = nyctalopia, atrophic patches seen

disease progression = atrophic lesions coalesce and move centripetally towards PP

4th-5th decade = macular involvement

What are 2 possible complications of gyrate atrophy?

dense PSC early in life (2nd decade)

CME

What are some systemic assocations seen with gyrate atrophy?

mild cognitive impairment

delayed language development/speech defects

thin, sparse hair

muscular atrophy

What is the tx for gyrate atrophy?

no cure, but reducing ornithine levels systemically can help with these 3 things:

low-protein, arginine-restricted diet

Vit B6

creatine

What is Stargardt disease?

mutation in ABCA4 gene = accumulation of visual cycle byproducts in RPE and PR death

What is the appearance of Stargardt disease?

pigment mottling

"beaten bronze" appearance of macular atrophy

Bullseye maculopathy

fundus flecks = pisciform shaped yellow-white dots of lipofuscin buildup

How does Stargardt disease appear on FAF?

hyperAF of flecks (increased lipofuscin)

hypoAF of RPE damage

How does Stargardt disease appear on IVFA?

dark choroid due to extreme accumulation of lipofuscin in the RPE that blocks underlying choroid

hyperfluorescent flecks that stain

What are some diagnostic tests we can do for Stargardt disease?

OCT = PR atrophy

ERG and EOG = abnormal in later stages

What are some symptoms of Stargardt disease?

bilateral central VA loss

photophobia

color vision anomalies

central scotomas

slow dark adaptation

What is the evolution of Stargardt disease?

onset usually between childhood or early adulthood, starting at 20/20-400

rapid vision detioriation that can preceed fundus appearance

What is fundus flavimaculatus, which is on the Stargardt spectrum?

condition that has...

later onset of the disease

slower detiorioration of vision

more widespread retinal involvment

macula less involved = better VA

What is the tx for Stargardt disease?

photoprotection as bright light can lead to formation of all-trans-retinal in PR's and contribute to further lipofuscin accumulation

LV referral