q banks power Flashcards

1
Q
Kid with:
reduced vocabulary for age
incorrect understanding of a word's meaning, 
 incorrect grammar use.
Dx?
A

Language disorder

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2
Q

What’s the difference between Language disorder and Childhood-onset fluency disorder?

A

Language disorder has no trouble with fluency.

Childhood-onset fluency disorder is all about not having fluency= STUTTERING

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3
Q

Kid with
difficulties in sound articulation, can result in irritability and frustration and a reluctance to engage in conversations.
Dx

A

Speech sound disorder

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4
Q

the triad of dysphagia, upper esophageal webs, and iron deficiency anemia
Dx?

A

Plummer-Vinson syndrome

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5
Q

How would you treat a DKA kid, with serum

K+>5.3?

A

IV 0.9% saline + insulin therapy

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6
Q

How would you treat a DKA kid, with serum

K+ <5.3 , >3.3?

A

IV solution + K repletion + insulin therapy

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7
Q

How would you treat a DKA kid, with serum

K+ <3.3?

A

K repletion BEFORE initiating insulin

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8
Q

What kind of hyponatremia produces Hydrochlorothiazide ?

A

hypovolemic, hypotonic hyponatremia

through natriuresis.

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9
Q

What kind of hyponatremia produces Cerebral salt wasting syndrome,

A

hypovolemic, hypotonic hyponatremia

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10
Q

Euvolemic hypotonic hyponatremia in the context of recent neurosurgery is suggestive of

A

Syndrome of inappropriate antidiuretic hormone secretion (SIADH)

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11
Q

kid with, short stature, obesity, big appetite, developmental delays, tantrums, cryptorchidism/ hypogonadism. think about? dx?

A

Prader-Willi Syndrome

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12
Q

Low birth weight, microcephaly (head circumference at the 2nd percentile), microphthalmia, polydactyly, cleft lip and palate, and rocker-bottom feet (convex foot deformity with prominent heel) are strongly suggestive of

A

trisomy 13, patau syndrome

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13
Q

the 7 Ps of Patau Syndrome are:

A
  • holoprosencephaly
  • cleft liP & Palate
  • Polydactyly
  • Pump disease (heart)
  • Polycystic kidney D
  • cutis aPlasia
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14
Q

Patau syndrome is caused the trisomy of:

A

13

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15
Q

Edward Sx

PRINCE means?

A

PRINCE Edward turned 18:

  • Prominent occiput
  • Rocker-bottom feet,
  • Intellectual disability,
  • Nondisjunction (in meiosis)
  • Clenched fists, low-set …
  • Ears,
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16
Q

47, XYY syndrome and 47, XXX syndrome. Common clinical features?

A

Tall Stature
Delays in motor and language development
+-fertility problems

Men: +-sever acne

17
Q

Cri-du-chat syndrome.

Cause and Cxfx

A

deletion on the short arm of chromosome 5.

  • **cat-like, high-pitched crying
  • Microcephaly
  • epicanthal folds
18
Q

Rett syndrome classically would present ass:

A

a girl that has achieved her milestones, but at 6-18 months has regressions in all domains
+ Seizures
“el retroceso”

19
Q

+ Envelope antigen for HepB is indicative of

A

activity of the disease “Ective”

20
Q

IgG Core antigen for HepB is indicative of

A

Chronic

C,C