13. Renal Disease Flashcards

1
Q

What is azotemia?

A

Build up of nitrogenous products in blood

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2
Q

What are the common findings of chronic renal failure?

A

*Pruritis
Vomiting
Muscle twitches and cramps

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3
Q

What are the 2 most important labs for diagnosing chronic renal failure?

A

BUN

Creatinine

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4
Q

What is the most common ocular finding of chronic renal failure?

A

Band K

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5
Q

What is te most common nephrotic syndrome?

A

Diabetic nephropathy

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6
Q

What causes diabetic nephropathy?

A

Glomerular sclerosis and fibrosis from metabolic changes in DM

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7
Q

How is an albumin screening done?

A

24 hour urine analysis

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8
Q

Nephropathy occurs how long after onset of DM?

A

10 years

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9
Q

Renal failure occurs how long after nephropathy?

A

10 years

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10
Q

What is the Alport syndrome triad?

A

Hereditary nephritis
Deafness
Ocular anomalies

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11
Q

Alport syndrome includes a basement membrane disorder specific to what?

A

Renal glomeruli

  • Cochlea
  • Retina
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12
Q

What is the hallmark anterior seg finding in Alport syndrome?

A

Anterior lenticonus

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13
Q

What are the ocular findings in Alport syndrome?

A

PDS
Anterior lenticonus
Retinal flecks
May have S and P fundus

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14
Q

What are the three forms of aniridia syndrome associated with Wilm’s tumor?

A

AN1
AN2
AN3

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15
Q

What are the findings of AN1?

A

Only ocular

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16
Q

What are the findings of AN2?

A
WAGR complex (includes the following):
Wilm's tumor
Aniridia
genitourinary anomalies
Mental retardation
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17
Q

What are the findings of A3?

A

AR
Aniridia
Mental deficiency
Ataxia

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18
Q

What should happen to respiratory rate in lactic (metabolic) acidosis?

A

Increased respiratory rate

19
Q

What is Phenylketonuria?

A

Inability to metabolize phenylalanine to tyrosine

20
Q

What is the most common systemic finding of phenylketonuria?

A

Mousy body odor

21
Q

What organs does amyloidosis affect?

A

Heart
Kidneys
Adrenals
Liver

22
Q

What are the systemic findings of amyloidosis?

A

Cutaneous hemorrhages - bloodhound appearance

23
Q

When is secondary amyloidosis seen?

A

After chronic infectious or inflammatory disease (TB, leprosy, RA, AS, IBS)

24
Q

What are the common ocular findings of secondary amyloidosis?

A

Prominent corneal nerves

“string of pearls” vitreous

25
What is Meretoja Syndrome?
Familial amyloidosis and corneal lattice dystrophy 2
26
What is Gaucher's disease?
Products of fat metabolism depositied in bone marrow
27
What are the ocular findings of Gaucher type 1?
Severe uveitis
28
What are the ocular findings of Gaucher type 2?
Blindness | Cherry red spot
29
What is Neiman-Pick?
Build up of sphingo-myelin or cholesterol in the tissues
30
What are the common findings of Nieman-Pick?
Cherry red spot Corneal opacities Brown lens capsule Peri-foveal crystalloid deposits in adults
31
What things cause a cherry red spot?
Methanol poisoning Quinine poisoning Dapsone toxicity Storage diseases
32
What are the causes of acidosis with elevated anion gap?
Ketoacidosis | Intoxication
33
What is the important cause of acidosis with a normal anion gap?
Acetazolamide
34
What drug type can cause chloride responsive alkalosis?
Diuretics
35
What drug type can cause chloride resistant alkalosis?
Loop diuretics | Thiazides
36
What causes cystinosis?
Error of amino acid metabolism
37
What causes Fanconi syndrome?
Defective carrier mediated transport of cystine
38
What is the common problem caused by Fanconi syndrome?
Progressive renal dysfunction
39
All 3 types of Fanconi present in the cornea how?
As crystals
40
Which type of cystinosis presents with symptomatic corneal crystals?
Infantile nephropathic cystinosis
41
Homocystinuria is a metabolic disorder of what?
The amino acid methionine
42
Homocystinuria is toxic to endothelial cells, causes what?
Increased platelet adhesion
43
Because of the increased platelet adhesion, homocystinuria has a higher risk of what?
Thrombus formation
44
What are the common ocular findings of homocystinuria?
``` Blue sclera Ectopia lentis Cataracts high myopia CRA occlusion ```