Pathology Volume 3 Flashcards

1
Q

What type of collagen is associated with Descemet’s membrane?

A

Type IV collagen

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2
Q

What is the most common inheritance pattern of CHED?

A

Autosomal recessive

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3
Q

What is the most common ocular association of sclerocornea?

A

Cornea planus

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4
Q

Of the classic corneal stromal dystrophies, which is autosomal recessive?

A

Macular dystrophy

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5
Q

What causes corneal whorls?

A

Deposition of lysosomal deposits within the basal layer of the epithelium

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6
Q

What chromosome is associated with macular dystrophy?

A

16q

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7
Q

What chromosome is associated with granular. Lattice and Avellino dystrophy?

A

5q

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8
Q

What causes corneal guttae?

A

Focal thickening of Descemet’s membrane

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9
Q

What condition is associated with PITX2 gene?

A

Axenfeld-Rieger syndrome

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10
Q

What is Axenfeld anomaly?

A

Posterior embryotoxon and iris adhesions to the cornea

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11
Q

What is Axenfeld syndrome?

A

Axenfeld anomaly plus glaucoma

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12
Q

What is Rieger anomaly?

A

Axenfeld anomaly plus iris atrophy

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13
Q

What is Rieger syndrome?

A

Rieger anomaly plus dental and skeletal abnormalities

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14
Q

What is thought to cause pigment dispersion syndrome?

A

Rubbing of the iris pigment epithelium by lens zonules

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15
Q

Name 3 systemic associations of exfoliation syndrome.

A
  1. Hypertension 2. Stroke 3. Myocardial infarction
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16
Q

What does angle recession represent histologically?

A

Tear in the ciliary body between the longitudinal and circular muscles

17
Q

Name 3 ocular complications of nanopthalmos.

A
  1. Hyperopia 2. Glaucoma 3.Uveal effusion syndrome
18
Q

Name the 3 layers of the sclera.

A
  1. Episcleral 2. Stroma 3. Lamina fusca
19
Q

What condition is associated with proliferation of spindle calls in a storiform pattern?

A

Fibrous histiocytoma

20
Q

How is the sclera altered in nanopthalmos?

A

Sclera is abnormally thick in nanopthalmos

21
Q

What is the most common location of senile calcific plaques?

A

Anterior to the lateral and medial rectus muscles

22
Q

What structures represent the tertiary vitreous?

A

Zonular fibers

23
Q

What does Bergmeister papilla represent?

A

Remnant of the posterior portion of the hyaloid artery

24
Q

What is the most common location of Mittendorf dot?

A

Inferonasal posterior capsule

25
What disorder is associated with "candlewax drippings" of the retinal vasculature?
Sarcoidosis
26
In what layer of the retina do cystic spaces occur in typical peripheral cystoid degeneration?
Outer plexiform layer
27
In what layer of the retina do cystic spaces occur in reticular peripheral cystoid degeneration?
Nerve fiber layer
28
What protein is associated with amyloid deposits of the vitreous?
Transthyretin
29
What condition is associated with amyloid deposits of the vitreous?
Familial amyloid polyneuropathy
30
What is the most common location of degenerative retinoschisis?
Inferotemporal
31
Where does reticular peripheral cystoid degeneration occur?
Posterior to areas of typical peripheral cystoid degeneration
32
What is the most common type of degenerative retinoschisis?
Reticular degenerative retinoschisis
33
What causes the clinical appearance of cobblestone degeneration?
Adherence of the inner nuclear layer to Bruch's membrane
34
What do cytoid bodies represent?
Swollen NFL axons