"Most commons" + surprise Flashcards

1
Q

Most common genetic cause of MR

A

Down’s syndrome

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2
Q

2nd most common genetic cause of MR

A

Fragile-X syndrome

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3
Q

Most common cancer of the children

A

ALL

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4
Q

Most common lysosomal storage d/o

A

Gaucher disease

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5
Q

Most common germ cell tumor of the testis

A

Seminoma

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6
Q

Most common malignant germ cell tumor of the testis in infancy and early childhood

A

Endodermal sinus (yolk sac) tumor

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7
Q

Most common systemic vasculitides

A

Temporal arteritis

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8
Q

Most common acquired heart disease

A

Kawasaki disease

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9
Q

Most common cause of upper GUT hematuria

A

Renal stones

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10
Q

Most common cause of lower GUT hematuria

A

UTI

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11
Q

Most common non-infx lower GUT hematuria

A

Urothelial CA

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12
Q

Most common microscopic hematuria in adult males

A

BPH

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13
Q

Parameters involved in Acute Renal Failure 2ndary to renal cause

A

Urine Osm 20
FeNa >2%
BUN/ Crea ratio

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14
Q
CRF stage
polyuria
GFR =50%
Asymptomatic
Normal BUN, Crea
A

I: Diminished renal reserve

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15
Q

CRF stage
Polyuria
GFR =20-50%
(+) azotemia, HPN, anemia

A

II: Renal insufficiency

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16
Q

CRF stage
Oliguria
(+) uremia, edema, metab acidosis, hypoCa

A

III: Renal failure

17
Q

CRF stage
oliguria/anuria
GFR

18
Q

Congenital abN presenting w/ renal agenesis, club foot, and pulmo hypoplasia

A

Renal agenesis

19
Q

Congenital renal anomaly assoc w/ Turner syndrome

A

Horseshoe kidney

20
Q

Enlarged irreg kidneys w/ islands of undifferentiated mesenchyme; can be unilat or bilat

A

Cystic renal dysplasia

21
Q

Bilateral
Mutation in PKD (polycystin)
Assoc w/ extrarenal anomalies like berry aneurysm, HPN, MVP, cyst in liver, spleen, pancreas, lungs

A

Autosomal dominant polycystic kidney dse

22
Q
Bilat mostly
Mutation on Chr 6 (PKHD1-> fibrocystin)
(+) Spokes on wheel pattern
Smooth outside, spongy inside
Causes potter facies
A

Autosomal recessive PKD

23
Q

Multiple cystic dilation of CD in the medulla

Asymptomatic

A

Medullary sponge kidneys

24
Q

Cysts on the corticomedullary jx

progress to CRF in 5-10 yrs

A

Nephronophthisis- medullary cystic disease complex

25
Most common renal cyst; cortical
Simple cyst
26
Presents with cortical and medullary cysts Dialysis-related Complication: renal cell CA
Acquired cystic dse
27
LM: hypercellularity IF: granular deposits EM: Subepithelial humps
PSGN
28
LM: Crescent formation IF: Linear deposits EM: GBM disruption
RPGN
29
LM: Capillary wall thickening IF: Granular IgG and C3 EM: Spike and dome
Membranous Glomerulopathy
30
EM: Effacement of foot processes
Minimal change disease
31
LM: Tram track IF: Granular EM: Type I - subendothelial deposit Type II - intramembranous deposit
MPGN
32
LM: Focal sclerosis and hyalinosis IF: Focal deposits of IgM, C3 EM: Loss of foot processes, epith denudation
Focal segmental glomerulosclerosis (FSGS)
33
LM: Mesangial widening and proliferation IF: Mesangial deposits EM: Mesangial deposits
IgA nephropathy
34
Most common cause of nephritic syndrome in children
PSGN
35
Most common cause of nephrotic syndrome in children
Minimal change disease
36
Most common cause of nephrotic syndrome in adults
FSGS
37
Most common GN overall
IgA nephropathy
38
Most common cause of ARF
Acute tubular necrosis
39
Most common cause of Chronic renal failure
Diabetes mellitus