Chapter 37- Alterations of Renal and Urinary Tract Function in Children Flashcards

1
Q

Poststreptococcal glomerulonephritis in children:

a. is a post infectious renal disease
b. causes hypotension
c. causes dehydration
d. both B & C are correct

A

a. is a post infectious renal disease

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2
Q

Infants cannot concentrate urine because of:

a. shorter tubular length
b. increase tubular weight
c. increased blood flow to the kidneys
d. both a & c are correct
e. a, b, c are correct

A

d. both a & c are correct

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3
Q

Vesicoureteral reflux causes urine to ____ up the ureters and places the young child at risk for ______

a. retrograde, glomerulonephritis
b. regrade, nephrotic syndrome
c. retrograde, pyelonephritis
d. regrade, cystitis

A

c. retrograde, pyelonephritis

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4
Q

IgA nephropathy:

a. occurs in the presence of other systemic immunologic disease
b. has no other immunoglobulin present
c. damages the glomerulus irreversibly
d. manifests as recurrent gross hematuria

A

d. manifests as recurrent gross hematuria

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5
Q

Organic causes of enuresis may include:

a. congenital abnormalities of the urinary tract
b. a neurologic origin
c. diabetes insipidus
d. all of the above are correct

A

d. all of the above are correct

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6
Q

Which clinical manifestations suggests hemolytic uremic syndrome?

a. polyuria
b. pallor and bruising
c. hypotension
d. all of the above are correct

A

b. pallor and bruising

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7
Q

Childhood urinary tract infection results from:

a. bacteria ascending up the ureter in cystitis
b. bacteria ascending up the urethra in pyelonephritis
c. detrusor muscle hypoactivity
d. a pathogenic strain of e. coli

A

d. a pathogenic strain of e. coli

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8
Q

Wilms tumor is characterized by:

a. hypotension
b. diagnosis in early teens
c. loss or inactivation of both copies of Wilms tumor suppressor genes
d. transmission in an autosomal recessive fashion for inherited cases

A

c. loss or inactivation of both copies of Wilms tumor suppressor genes

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9
Q

Childhood nephrotic syndrome is characterized by

a. having peak incidence during the teen years
b. increased glomerular permeability to protein
c. hypolipidemia
d. injured renal interstitial tissue

A

b. increased glomerular permeability to protein

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10
Q
1. Which of the following is NOT a complication of the horseshoe kidney?
A. Hydronephrosis
B. Hypospadias
C. Infection
D. Stone formation
A

B. Hypospadias

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11
Q
2. A 2-month-old male infant presents with the urethral opening on the dorsal surface of the penis. Which of the following is the correct name for this anomaly?
A. Hypospadias
B. Epispadias
C. Exstrophy
D. Ureteropelvic junction
A

B. Epispadias

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12
Q
3. A person is born with abnormal differentiation of renal tissues. Which of the following medical terms describes this condition?
A. Renal aplasia
B. Hypoplastic kidney
C. Renal dysplasia
D. Renal agenesis
A

C. Renal dysplasia

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13
Q
4. A person presents with wide-set eyes, “parrot beak” nose, low-set ears, and receding chin. What is the renal manifestation associated with this presentation?
A. Potter syndrome
B. Polycystic kidney disease
C. Minimal change neuropathy
D. Hemolytic-uremic syndrome
A

A. Potter syndrome

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14
Q
  1. A 6-year-old has just recovered from streptococcal pharyngitis. Which of the following is TRUE regarding acute poststreptococcal glomerulonephritis?
    A. Antibody-antigen complexes of IgM, IgG, and IgA are deposited.
    B. The exact mechanism of immune complexes is unknown.
    C. There is decreased vascular permeability.
    D. There are no signs of inflammation.
A

B. The exact mechanism of immune complexes is unknown.

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15
Q
6. An individual presents with hematuria, proteinuria, and abdominal pain. There are also skin lesions. Which of the following diseases does this represent?
A. Henoch-Schönlein purpura
B. Hemolytic uremic syndrome
C. Primary nephrotic syndrome
D. Minimal change nephropathy
A

A. Henoch-Schönlein purpura

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16
Q
  1. What is the cause of minimal change nephropathy?
    A. Fusion of the glomerular foot processes
    B. Verotoxin of Escherichia coli
    C. IgA deposition
    D. Inflammation of the glomeruli
A

A. Fusion of the glomerular foot processes

17
Q

Urine formation and excretion begin by the _________ month of gestation.

A

third

18
Q

Genetically, the ________ plays an important role at all stages of kidney development.

A

Wilms tumor gene 1

19
Q

During the first year of life, infant’s GFR is about ______ of adult levels.

A

30-50%

20
Q

The primitive glomeruli and uriniferous tubules develop from the _______.

A

metanephrogenic blastema

21
Q

An infant has a lower threshold for bicarbonate reabsorption and limited acid excretion, this increases the risk for developing _________.

A

metabolic acidosis

22
Q

When a child has had and then loses bladder control, it is know as ________.

A

secondary enuresis

23
Q

A __________ kidney is a small but normal functioning organ.

A

dysplastic

24
Q

__________ is blockage where the renal pelvis joins the ureter.

A

Utereropelvic junction obstruction

25
Q

_______ exhibits a urethral meatus on the ventral surface of the penis.

A

Hypospadias

26
Q

Urine seepage onto the abdominal wall from the ureter can observed in ________.

A

exstrophy of the bladder

27
Q

Polycystic kidney disease is an autosomal ______ disorder.

A

dominant

28
Q

Bilateral renal agenesis is usually ________.

A

fatal

29
Q

Congenital malpositioning of a ureter or ureters into the bladder causes _______.

A

primary vesicoureteral reflux

30
Q

________ is responsible for most school-aged children who require dialysis and kidney transplantation.

A

Chronic glomerulonephritis

31
Q

Common childhood glomerular disease include glomerulonephritis, hemolytic uremic syndrome, and _______.

A

nephrotic syndrome