peds103 Flashcards

(49 cards)

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

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

25
neonate with cataracts only
galactokinase def
26
neonate with cutaneous lesions on the palms and soles, hepatosplenomegaly, jaundice, anemia, and rhinorrhe
congenital syphilis
27
late congenital manifestations of syphilis
present after two years of age; frontal bossing, high arched palate, hutchinson teeth, intersitialkeratitis, saddle nose, and perioral fissures
28
treatment for syphilis
parenteral penicillin G
29
hepatosplenomegaly, hydrocephalus, chorioretinisit, and intracranial calcifications
congenital toxo
30
sensorineural hearing loss, cataracts, heart defects, hepatosplenomegaly, petechiae or purpura (blueberry muffin)
congenital rubella
31
IUGR, hepatosplenomegaly, petechiae or purpura, microcephaly, chorioretinitis, sensorineural hearing loss, and periventricular calcifications
congenital CMV
32
xray of baby born with congenital syphilis
metaphyseal dystrophy and periositis
33
fever, odynophagia/dysphagia, drooling, neck siffness, muffled voice, and unable to open the mouth completely
infection of the larynx, pharynx, or deep neck space
34
what imaging to see retropharyngeal abscess
CT with contrast
35
difference in the dishcarge of chlamdia and gon conjunctivitis?
chlamyd is more watery, mucoud discharge and less purulent than gonococcla
36
how to prevent gonoccocal conjunctivitis
topical erythromycin within 1 hours of birth
37
most common type of leukmia in kids
ALL
38
lymphoblasts that lack peroxidase positive granules but often contain cytoplasmic aggregates of periodic acid Schiff pos material (PAS)
ALL
39
peroxidase pos material
in myeloblasts
40
histologic starry sky appearance
burkitt lymphoma (which responds well to chemo due to high mitotic rate
41
auer rods
acute myelocytic leukemia (AML)
42
myelodysplastic syndromes
clonal stem cell disorders which may progress to acute leukemias; usually seen in elderly patients and characterized by pancytopenia
43
TdT positive staining
expressed only by pre B and pre T lymphoblasts
44
recurrent sinopulm infections, oral candidiasis, persistent diarrhea, opportunistic infection and viral infections
SCID
45
absent lymph nodes and tonsils, lymphopenia, absent thymic shadow on chest xray, and abnormal T, B, and natural killer cell enumeration
SCID
46
common variable immunodeficiency is the same as
acquired hypogammaglobinemia
47
CVID
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
x-linked agammaglobineumia
aka Bruton's agammaglobinemia
49
male infant who is initially asymptomatic until 6-9 mo, when he begins to have recurrent Strep pneumo or H flu infections
Bruton's agammaglobinemia