peds103 Flashcards

1
Q

diff between umbilical hernia, oomphalocele, and gastroschesis

A

umbilical hernia covered by skin, oomphalocele covered by peritoneaum, gastroschesis uncovered intestines (always to the right)

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2
Q

simple febrile seizure

A

nonfocal (tonic-clonic or atonic), one episode less than 15 mins or multiple less than 30 mins

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3
Q

complex febrile seizure

A

focal, one episode greater than 15 mins or multiple greater than 30 mins

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4
Q

management of febrile seizure

A

abortive therapy if seizure greater than 5 mins, reassurance/education; brain imaging can be considered in complex febrile seizure only

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5
Q

prognosis for febrile seizures

A

normal development/intelligence; 30% risk of recurrence, less than 5% risk of epilepsy

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6
Q

age for febrile seizures

A

6 mos to 6 years

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7
Q

recurrent URI, persistent nasal drainage, and nasal polyps

A

rule out CF

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8
Q

2 yo how many words

A

200 words

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9
Q

builds a tower of 6 cubes

A

2 years

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10
Q

walks down and up stairs, jumps, throws a ball overhead

A

2 years

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11
Q

follows two step commands, removes clothes

A

2 years

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12
Q

copies a circle, uses utensils, stacks 9 blocks

A

3 yo

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13
Q

climbs stairs with alternating feet

A

3 yeas

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14
Q

rides a tricycle

A

3 years

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15
Q

states first name

A

3 yo

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16
Q

washes/dries hands

A

3 yo

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17
Q

draws a person, begins to use sciessors, holds crayon with tripod grasp

A

4 yo

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18
Q

hops on one foot without losing balance

A

4 yo

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19
Q

counts to 10

A

4 yo

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20
Q

tells stories, uses plurals and prepositions

A

4 yo

21
Q

klumpke palsy

A

c8, t1 are injured; forearm pronators, wrist flexors, and dilators of the iris and elevators of the eyelid ; claw hand; moro intact; grasp reflex absent

22
Q

erb-duchenne palsy

A

most common type of brachial plexus injury and involves the C5 and C6; leads to waiter’s tip posture; grasp reflex intact; may have decreaed or absent moro reflexes

23
Q

newborn with failure to thrive, bilateral cataracts, jaundice, and hypoglycemia

A

galactosemia, caused by galactose-1-phosphate uridyl transferase def, leading to elevated galactose in the blood

24
Q

aminoaciduria, hepatic cirrhosis, hypoglycemia, and mental retard

A

galactosemia

25
Q

neonate with cataracts only

A

galactokinase def

26
Q

neonate with cutaneous lesions on the palms and soles, hepatosplenomegaly, jaundice, anemia, and rhinorrhe

A

congenital syphilis

27
Q

late congenital manifestations of syphilis

A

present after two years of age; frontal bossing, high arched palate, hutchinson teeth, intersitialkeratitis, saddle nose, and perioral fissures

28
Q

treatment for syphilis

A

parenteral penicillin G

29
Q

hepatosplenomegaly, hydrocephalus, chorioretinisit, and intracranial calcifications

A

congenital toxo

30
Q

sensorineural hearing loss, cataracts, heart defects, hepatosplenomegaly, petechiae or purpura (blueberry muffin)

A

congenital rubella

31
Q

IUGR, hepatosplenomegaly, petechiae or purpura, microcephaly, chorioretinitis, sensorineural hearing loss, and periventricular calcifications

A

congenital CMV

32
Q

xray of baby born with congenital syphilis

A

metaphyseal dystrophy and periositis

33
Q

fever, odynophagia/dysphagia, drooling, neck siffness, muffled voice, and unable to open the mouth completely

A

infection of the larynx, pharynx, or deep neck space

34
Q

what imaging to see retropharyngeal abscess

A

CT with contrast

35
Q

difference in the dishcarge of chlamdia and gon conjunctivitis?

A

chlamyd is more watery, mucoud discharge and less purulent than gonococcla

36
Q

how to prevent gonoccocal conjunctivitis

A

topical erythromycin within 1 hours of birth

37
Q

most common type of leukmia in kids

A

ALL

38
Q

lymphoblasts that lack peroxidase positive granules but often contain cytoplasmic aggregates of periodic acid Schiff pos material (PAS)

A

ALL

39
Q

peroxidase pos material

A

in myeloblasts

40
Q

histologic starry sky appearance

A

burkitt lymphoma (which responds well to chemo due to high mitotic rate

41
Q

auer rods

A

acute myelocytic leukemia (AML)

42
Q

myelodysplastic syndromes

A

clonal stem cell disorders which may progress to acute leukemias; usually seen in elderly patients and characterized by pancytopenia

43
Q

TdT positive staining

A

expressed only by pre B and pre T lymphoblasts

44
Q

recurrent sinopulm infections, oral candidiasis, persistent diarrhea, opportunistic infection and viral infections

A

SCID

45
Q

absent lymph nodes and tonsils, lymphopenia, absent thymic shadow on chest xray, and abnormal T, B, and natural killer cell enumeration

A

SCID

46
Q

common variable immunodeficiency is the same as

A

acquired hypogammaglobinemia

47
Q

CVID

A

manifest at later age (15 yo), serum concentrations of IgG, IgA, IgM and IgE may be decreased; NO absence or decrease in the number of B cells

48
Q

x-linked agammaglobineumia

A

aka Bruton’s agammaglobinemia

49
Q

male infant who is initially asymptomatic until 6-9 mo, when he begins to have recurrent Strep pneumo or H flu infections

A

Bruton’s agammaglobinemia