Blue 3-1 Flashcards

(27 cards)

1
Q

What is the prevalence of childhood amblyopia <0.3

A

1%

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2
Q

What is the mortaility rate among children in the year following diagnosis of severe visual impariment

A

10%

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3
Q

When is annual age group specific incidenc eo fchildhood visual impairment hightest

A

First year of life

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4
Q

What are most common causes of severe visual impairment in children in the UK

A

Cerebral visual impairment
opitc nerve disorder

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5
Q

What is sturge Weber sydnrome? Wjhat gene? What ocular abnormlaiteis? Which side?

A
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6
Q

When to treat ROP

A

Zone 1 any stage with plus dusease

Zone 1 stage 3+ without plus disease

Zone 2 stage 3+ with plus disase

Consider in zone 2 stage 2 with plus disease

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7
Q

ROP stages

A

DRFIT
1 - demarcation line
2 - ridge
3 - fibrovascular changes
4 - incomplete RD 4a mac on 4b mac off
5 - total RD

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8
Q

ROP zones

A

1 twice width of disc to fovea areound disc

2 up to nasal ora around disc

3 temporal crescent

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9
Q

CRYO ROP

A

Threshold ROP
Zone I/II
Plus disease
Stage 3
5 continuous or 8 non-continous clock hours

Cryo in threshold ROP reduces risk of RD/macular fold/retrolental mass by 50%

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10
Q

ETROP

A

Prethreshold ROP:
Zone 1 any stage with plus
Zone 1 stage 3 without plus
Zone 2 stage 2 or stage 3 with plus

  • Early laser reduce risk of adverse outcomes
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11
Q

What are diagnostic criteria for congenital infantile esotropia

A

Esotropia 40-50PD with a range of 10-90PD

Normal neurological status

Refractive error expected for age
(low to moderate hyperopia) correction of which does not eliminate esotropia

Asymmetric optokinetic nystagmus with robus temporal to nasal response and erratic nasal to temporal response

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12
Q

Stickler syndrome which type is associated with ocular problems?
Inhertiance patter?
Collagen type?

A

STL1 stickler type 1
COL2A1 (type 2 collagen)
Type 3 non ocular

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13
Q

When should congenital cataract be removed

A

6 weeks for single cataract
10 weeks for two (bilateral)

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14
Q

Inheritance of posterior polar cataract?

A

Autosomal dominance

Associated with mutations in PITX3

PErsistent fetal vasculature can be assocaited with posterior plaque outside or involving the posterior capsule of clear lens

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15
Q

What is posterior lenticonus?

A

Central/paracentral posterior capsule is thin and bulges posteriorly

Occurs at the location where the hyaloid system attaches to the eye

Localised area of extreme myopic refraction

Optical distortion
Unilateral mostly
Spontenous rupture of the lens is rare leading to total cataract

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16
Q

What are variable angle of deviation strabismus

A

Uncorrected refractive error
Anisometropia
Nystagmus compensation syndrome
Convergence excess esotropia

17
Q

What is microtropia

A

Small manifest deviation with a degree of BSV created by abnormal reitnal correspondence, eccentric fixation and a central suppression scotoma.

Microtropia with identity - no movement on cover test

Microtropia without identitiy - movement on cover test as eccentric fixation is not absolute

18
Q

What is eccentric fixation

A

Using part of retina other than fovea to fixate on an object - unconscious
Usually in amblyopia

19
Q

What is nystagmus blockage syndrome?

A

Esotropia developed to suppress congenital nystagmus

20
Q

What is convergence excess esoptropia?

A

Eyes converge more at near than at distance due to excessive accommodative convergence

> 10PD difference

High AC/A ratio

ManagementL
+2 to +3 bifocals to relax accommodation at near

Medial rectus recession

21
Q

What are indications for surgery in Duane syndrome

A

Elimination or improvement of an unacceptable head turn - success in 79-100%

Elimination or reduction of significant misalignment of the eyes

Reduction of severe retraction

Improvement of upshoots and downshoots

Does not improve fusion or motility

22
Q

Duane type I, II, III

A

I abDuction deficit - mild retraction - eso

II aDDuction deficit - severe retraction -exo

III abDuction and aDDuction deficit - moderate retraction - eso

23
Q

What mutation seen in x linked juvenile retinoschisis

A

RS1 mutation in 90-95%

24
Q

What is XLJR

A

Abnormality in intracellular adhesion molecule resulting in retinal splitting at the NFL in boys and may present with maculopathy

Foveal changes - stellate spoke like appearance with microcysts.

25
ERG in XLJR
Electronegative ERG responses Normal a wave Reduced b wave Focal, macular and full field ERG have similar results - widespread reitnal dysfunction
26
OCT/FFA in XLJR Treatment?
Cystic spaces in IN and OP layer sof retina No leakage on FFA MAcular microcysts respond to 2% dorzolamide
27
What happens in primary congenital glaucoma
Angle dysgenesis causes reduced aqueous outflow From birth to tenth year of life Bilateral