Hereditary and Chronic GN Flashcards

(15 cards)

0
Q

What other disturbances are associated with Alport syndrome than GN?

A

Nerve deafness, Visual disturbances, nephritis

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1
Q

What is the most common inheritance pattern of Alport syndrome?

A

X-linked recessive (most cases)

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2
Q

What does microscopy of Alport syndrome look like?

A

Glomeruli with segmental proliferation or sclerosis, mesangial matrix increase
Foam cells
Persistence of fetal glomeruli

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3
Q

What does EM of Alport syndrome look like?

A

Lamina densa splitting

NOT FOCAL

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4
Q

What is the gene defect in Alport syndrome?

A

Type IV collagen

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5
Q

What is the course of alport syndrome?

A

Renal failure in 20-50 years

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6
Q

What is the inheritance pattern of thin membrane disease (Benign Familial Hematuria)

A

Autosomal

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7
Q

What is the course outcome of thin membrane disease?

A

Excellent if Heterozygous

Homozygous may progress to renal failure

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8
Q

What is the defective gene in Thin membrane disease?

A

Type IV collagen

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9
Q

What of the GN diseases discussed can present to Chronic GN? (in order)

A
  1. RPGN
  2. Focal GS
  3. Membranous AND MPGN
  4. IgA nephropathy
  5. PSGN
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10
Q

What immune complexes are seen in SLE Nephropathy?

A

ALL OF THEM.

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11
Q

What are the stages of Lupus Nephritis?

A

I: Normal
II: Mesangial involvement
III: Focal proliferative (Some proteinuria and hematuria)
IV: Diffuse proliferative (Hematuria and severe proteinuria)
V: Membranous GN (Severe proteinuria)

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12
Q

What are some microscopic findings in diabetic nephropathy?

A

Basement membrane thickening
Mesangial sclerosis
Nodular glomerulosclerosis

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13
Q

What is nodular glomerulosclerosis associated with?

A

Kimmelstiel wilson nodules (hyaline masses in periphery of glom)

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14
Q

What is the clinical course of diabetic nephropathy?

A
Microalbuminuria
HTN
Diabetic nephropathy
ESRD
Dialysis/Kidney/Pancreas transplant
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