MIDTERM Flashcards

1
Q

Where does the AH produced?

A

From plasma by the ciliary epithelium of the ciliary body pars plicata

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2
Q

A sieve-like structure where 90% of AH leaves the eye

A

Trabecular meshwork

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3
Q

the innermost portion, consisting of cord-like endothelial cell-covered strands arising from the iris and ciliary body stroma

A

Uveal meshwork

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4
Q

lies external to the uveal meshwork to form the thickest portion of the trabeculum.

A

Corneoscleral meshwork

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5
Q

the outer part of the trabeculum and links the corneoscleral meshwork with the endothelium of the inner wall of the canal of Schlemm

A

Cribriform meshwork

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6
Q

a circumferential channel within the perilimbal sclera.

A

Schlemm canal

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7
Q

aqueous flows through the trabeculum into the Schlemm canal and then the episcleral veins.

A

Trabecular outflow

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8
Q

aqueous passes across the face of the ciliary body into the suprachoroidal space and is drained by the venous circulation in the ciliary body, choroid and sclera.

A

Uveoscleral drainage

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9
Q

the balance between the rate of aqueous production and the rate of aqueous outflow.

A

IOP

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10
Q

Normal range of IOP for adults

A

21 mm Hg

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11
Q

upper range of IOP for 70 years old

A

23 mmHg

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12
Q

AO is obstructed by a membrane covering the trabeculum

A

Pre trabecular

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13
Q

obstruction as a result of “clogging up” of the meshwork

A

Trabecular OAG

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14
Q

the trabeculum itself is normal but aqueous outflow is impaired as a result of elevated episcleral venous pressure.

A

Post trabecular OAG

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15
Q

Contact applanation tonometer
Newest form

A

Goldmann tonometer

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16
Q

Portable contact applanation tonometer

A

Perkins tonometer

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17
Q

It is used to measure the IOP

A

Tonometer

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18
Q

Oldest form
Contact indentation tonometer

A

Schiotz tonometer

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19
Q

Non-contact indentation tonometer

A

Air-puff tonometer

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20
Q

Portable non-contact applanation tonometer

A

Pulsair 2000

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21
Q

Portable contact applanation tonometer

A

Tono-pen

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22
Q

Used to visualize the angle structures of the eye

A

Goniolenses

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23
Q

Single or triple mirror
Contact surface diameter 12 mm
Suitable for ALT
Not suitable for indentation gonioscopy

A

Goldmann

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24
Q

Four mirror lens
Contact surface diameter 9mm
Not suitable for ALT
Suitable for indentation gonioscopy

A

Zeiss

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25
Anatomy of angle in order
Ciliar body Scleral spur Trabeculum Schwalbe line
26
Ciliary body easily visible
Grade 4
27
At least scleral spur is visible
Grade 3
28
Only trabeculum visible Angle closure possible but unlikely
Grade 2
29
Only schwalbe line and perhaps top of trabeculum visible
Grade 1
30
Iridocorneal contact Closed
Grade 0
31
Maximal area of colour contrast
Pallor
32
Bending of small blood vessels crossing
Cupping
33
Measurement of visual field function
Perimetry
34
Secondary trabecular block open angle glaucoma Pseudo-exfoliative material Trabecular hyperpigmentation
Pseudoexfoliative glaucoma
35
Bilateral trabecular meshwork open angle glaucoma Common in myopic young men Krukenberg spindle and very deep AC Trabecular hyperpigmentation Fine granules
Pigmentary glaucoma
36
Common, secondary angle-closure glaucoma without pupil block Caused by rubeosis iridis
Neovascular glaucoma
37
Clinical features of neovascular glaucoma
Ischemic CRVO CRAO (uncommon) Long standing diabetes Carotid obstructive disease (uncommon)
38
Signs of advanced neovascular g
Severely reduced VA Severe rubeosis iridis Distortion of pupil Synechial angle closure
39
posterior synechia extending 360 degrees
Seclusio pupillae
40
Bowing of the peripheral iris
Iris bombè
41
a secondary open-angle glaucoma occurring in association with a hypermature cataract Deep AC floating white particles
Phacolytic glaucoma
42
Signs: Irregular widening of ciliary body band
Post traumatic angle recession glaucoma
43
A syndrome which typically affects one eye of a middle aged woman
Iridocorneal endothelial syndrome
44
3 clinical presentation of ICE:
Chandler’s syndrome Progressive iris atrophy Iris naevus
45
abnormal corneal endothelial appearance said to resemble hammered silver. Iris atrophy- 40% Corneal changes predominate
Chandler syndrome
46
characterized by iris changes including corectopia Iris atrophy in 100%
Progressive iris atrophy
47
Pupil malposition
Corectopia
48
characterized by either a diffuse naevus that covers the anterior iris, or by iris nodules Iris atrophy- 50%
Iris naevus
49
a rare condition typically affecting both eyes of an older patient
Iridoschisis
50
A rare genetically determined abnormality in the trabecular meshwork and AC angle resulting in increased IOP
PCG
51
Triad of symptoms for elevated IOP
Photophobia, epiphora, blepharospasm
52
1:10,000, 65% boys Most sporadic
PCG
53
Clinical features of PCG
Corneal eodema Break in descemets membrane Optic disc cupping Buphthalmos
54
Management for PCG
Goniotomy Trabeculotomy Tonometry
55
Bilateral but asymmetrical Glaucoma is uncommon Posterior embryotoxon
Axenfeld anomaly
56
characterized by the Rieger anomaly together with extraocular malformations that, as with the ocular features
Reiger syndrome
57
Corneal opacity with iris adhesion and lenticular adhesions
Peters Anomaly
58
Signs of aniridia
Partial absence Subtotal absence Synechial angle-closure-75% Lens subluxation
59
Autosomal dominant Isolated 85%
AN-1
60
Deletion of chromosome 11 13%
AN-2 (Miller syndrome)
61
Autosomal recessive 2% Mental handicap
AN-3 (Gillespie syndrome)