Nephrology Flashcards

(38 cards)

1
Q

Benign Familial Hematuria

A

Thin Basement Membrane Nephropathy

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2
Q

Management of Edema in Minimal Change Disease

A

salt restriction

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3
Q

Most Common Cause of Hydronephrosis in infancy

A

Ureteropelvic junction obstruction

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4
Q

Coca Colored Urine + Viral Illness

A

IgA Nephropathy

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5
Q

Calcium Oxalate crystals, think

A

ethylene glycol ingestion (antifreeze)

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6
Q

What is deposited in anti-GBM disease

A

IgG and C3

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7
Q

What age to repair a hydrocele

A

1 year of age

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8
Q

ARPKD Features

A

Potter facies
palpable kidneys
hepatic fibrosis

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9
Q

Treatment of urethral prolapse

A

estrogen cream

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10
Q

PIGN Complement Levels

A

Low C3

normal C4

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11
Q

Inguinal Hernias should be repaired…

A

at diagnosis

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12
Q

Urethrorrhagia

A

hematuria at the ending of urinating in boys

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13
Q

When to being screening of proteinuria in DM

A

T1DM 3-5 years

T2DM at time of diagnosis

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14
Q

Hypoplasia or abscence of patella
Dystrophic Nails
Renal Disease

A

Nail-Patella Syndrome

AD

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15
Q

Most Common Thrombosis Sites in Nephrotic Syndrome

A

Sagittal Sinus

Renal Vein

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16
Q

Aminoglycoside - mechanism of renal toxicity

17
Q

RTA That Causes Renal Stones

A

Type 1 - Distal

18
Q

Salt Losing Nephropathy w/o signs of nephritis or nephropathy

A

Juvenile Nephronophthisis

19
Q

Prune Belly Syndrome

A

Cryptoorchidism
Abscence of Abd Wall Musculature
Dilation of bladder/urethra/etc

20
Q

penile foreskin cannot be retracted =

21
Q

Most Common Cause of Bilateral Urinary Obstructions

A

Posterior Urethral Valves

22
Q

Toxocara canis

A

dog roundworm

23
Q

Most Specific Test for Acute EBV

A

Viral Capsid Antigen (VCA) IgM

24
Q

Prune Belly Associated with ?hydroamions

A

oligohydroaminos –> pulmonary hypoplasia

25
Elevated BP - 2017 Guidelines
BP > 95%tile | 13 years: >120/80
26
When to further evaluate hypospadias
undescended testes or ambiguous genitlaia
27
silk glove sign
think inguinal hernia
28
Liddle Syndrome
primary Na retention | HTN, hypokalemia
29
Bartters & Gitelman Syndromes
Barters - Loop, hypercalciuria, normal Mag | Gitelman - HCTZ, low Mag
30
RTA Type 1
distal defect, impaired H+ secretion | elevated pH
31
Causes of Type 1 RTA
Amp B, SLE, Sjogren
32
RTA Type 2
proximal defection, decreased bicarb resoprtion | acidic pH
33
Causes of Type 2 RTA
Fanconi Syndrome, Cystinosis
34
Causes of Type 4 RTA
obstructive nephropathy
35
Denys-Drash Syndrome
infant-onset nephrotic syndrome, renal failure by 3 years
36
Symptoms of Medullary Sponge Kidney
Frequent UTIs, hematuria, renal stones
37
Bardet-Beidel Syndrome
obesity, cystic dysplasia of kindey, retinitis pigmentosa
38
Liddle & Gordon Syndrome
HTN Liddle: pseudoaldosteronism Gordon: pseudohypoaldosteronism