Renal Diseases & Urine Metabolic Disorders Flashcards

1
Q

Immune complex deposition in Glomerular

membrane sue to Group A streptococcal infection

A

Acute Glomerulonephritis

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2
Q

Acute Glomerulonephritis - Findings

A

(+) ASO Titer

Dysmorphic RBCs, RBC cast

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3
Q

Rapidly Progressive Glomerulonephritis is the immune complex deposits in Glomerular membrane due to __________________

A

Systemic Immune Disorder

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4
Q

IgA Nephropathy

A

Berger’s Disease

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5
Q

Most common cause of glomerulonephritis

A

IgA Nephropathy

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6
Q

Anti-Glomerular Basement membrane Antibody (AGBA) in GBM and alveolar basement membrane

A

Goodpasture Syndrome

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7
Q

ANCA (Anti-Nuclear Cytoplasmic AutoAntibody) in vessel walls of lungs and glomerulus

A

Wegener’s granulomatosis

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8
Q

Nephrotic Syndrome

A

Disruption of shield of negativity - podocyte barrier

Massive - Lipiduria, Proteinuria

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9
Q

Nephrotic Syndrome- Findings

A

Fatty Casts
RTE Cells
Waxy Casts
Oval fat Bodies

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10
Q

Minimal Change Disease is due to disruption of shield of negativity due to ________________________.

A

Allergic and Immune reactions

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11
Q

Chronic Glomerulonephritis

A

Marked ↓ in renal function resulting to Renal Failure

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12
Q

Chronic Glomerulonephritis - Findings

A

Waxy Casts

Azotemia

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13
Q

Findings - Acute Tubular Necrosis

A

Odorless Urine
Bubble Cells
Granular Dirty Brown Cast (Methemoglobin)

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14
Q

Defective Reabsorption in PCT

A

Fanconi Syndrome

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15
Q

Fanconi Syndrome - Findings

A

Cystine Crystals

Glucosuria

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16
Q

Interstitial Disorders

Lower UTI:
Upper UTI:

A

Interstitial Disorders

Lower UTI: Cystitis
Upper UTI: Pyelonephritis

17
Q

Acute Interstitial Nephritis - Findings

A

NO BACTERIA

EOSINOPHILURIA (>1%)

18
Q

Acute Interstitial Nephritis is from the __________________

A

Renal Interstitium Allergic inflammation

19
Q

Most well-known aminoaciduria

A

PKU

20
Q

PKU

Odor:
Defective Gene:

A

PKU

Odor: Mousy/Musty Odor
Defective Gene: Phenylalanine Hydroxylase

21
Q

Tests for PKU

FeCl Tube Test:
2,4 Dinitrophenylhydrazine:
Phenistix:
Guthrie Test:

A

Tests for PKU

FeCl Tube Test - Blue Green
2,4 Dinitrophenylhydrazine - Yellow
Phenistix - Green Gray
Guthrie Test - B. subtilis growth

22
Q

Tyrosinemia

Odor:
Defective Gene:
 Type I
 Type II
 Type III
A

Tyrosinemia

Odor: Rancid
Defective Gene
 Type I - FAA: Fumarylacetoacetate
 Type II - TAT: Tyrosineaminotransferase
 Type III - p-HP: p hydroxyphenylpyruvic acid oxidase
23
Q

MSUD

Odor:
Defective Gene:

A

MSUD

Odor: Caramelized sugar/ maple syrup/ curry urine odor
Defective Gene: a-ketoacid decarboxylase

24
Q

MSUD blocks the normal metabolism of the three branching enzyme:

A

Leucine
Isoleucine
Valine

25
Q

Alkaptonuria

Defective Gene:
Urine Color:

A

Alkaptonuria

Defective Gene: Homogentisic acid oxidase
Urine Color: Dark Urine @ ROOM TEMPERATURE

26
Q

Dark Urine at _________ is present in Melanuria

A

Air exposure

27
Q

Cystinuria is due to defect in reabsorption of:

Mnemonics: COLA

A

Cystine
Ornithine
Lysine
Arginine

28
Q

Sweaty Feet Urine Odor

A

Isovaleric & Glutaric Acidemia

29
Q

Disorder due to Defective gene for Hypoxanthine Guanine Phosphoribosyl transferase

A

Lesch Nyan Syndrome

30
Q

Lesch Nyan Syndrome

Defective:
Inidcator:

A

Lesch Nyan Syndrome

Defective: Hypoxanthine Guanine Phosphoribosyl transferase
Inidcator: Orange Sand Paper

31
Q

No Cast

A

Cystitis

32
Q

No Bacteria

A

Acute Interstitial Nephritis

33
Q

WBC Cast

A

Acute Pyelonephritis

34
Q

RBC Cast and Dysmorphic RBCs

A

Acute Glomerulonephritis