Other Neurodevelopmental Deck (including ID) Flashcards

1
Q

what is a mnemonic for the Ericksonian stages

A
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2
Q

what is object permanence

A

concept from Piaget

a childs ability to know that objects continue to exist even though they can no longer be seen or heard

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3
Q

what is object permanence

A

concept from Mahler

psychodynamic term where the object is an “object of your affection”

occurs when the internalization of the relationship with the mother is adequate enough for the child to feel secure in the absence of the mother

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4
Q

before age 1, what emotional states exist in the child

A

negative–> distress

positive–> satiated

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5
Q

at what age do the primary emotions develop? what are these emotions

A

age 1

joy, anger, surprise, sadness, shyness, fear

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6
Q

when does the social smile develop

A

age 1-2 months

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7
Q

when do babies start to laugh out loud

A

4 months

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8
Q

when do babies start to laugh in response to games

A

7-9 months

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9
Q

when does stranger anxiety start and peak

A

starts around 4 months
peaks around 8-10 months
can last up to 18-24 months

separation anxiety starts at 8-10 months and peaks at 14-18 months

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10
Q

at what age do the “moral” or “self conscious” emotions start

A

age 2

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11
Q

what are two ways that children understand/regulate emotions

A
  1. social referencing
  2. joint attention
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12
Q

what is social referencing

A

using another person’s response to an ambiguous situation as a guide for one’s own response

by 1 year, infants are acutely sensitive to the emotional cues of other people

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13
Q

by what age does temperament become stable

A

4 months

impact of temperament on personality is dependent on “goodness of fit”

these characteristics persist throughout adulthood

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14
Q

in what % of cases of ID can you find a genetic etiology

A

40-50% of cases

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15
Q

list prenatal exposures that can result in ID

A

maternal DM

congenital rubella

CMV

syphillis

toxoplasmosis

herpes

AIDS

in utero EtOH expposure

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16
Q

list perinatal etiologies of ID

A

hypoxia

complications of prematurity

intra cerebral hemorrhage

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17
Q

list post natal causes of ID

A

deprivation, malnutrition

infections, toxins, trauma, inborn errors of metabolism

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18
Q

what is the rate of ASD in ID

A

10%

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19
Q

what is the age range for dx of GDD

A

under age 5

when clinical severity level cannot be reliably assessed

fails to meet expected developmental milestones in several areas of intellectual functioning

20
Q

which gene is responsible for Fragile X

A

mutation of FMRI gene
–> CGG trinucleotide repeats in of more than 200-230 repeats

21
Q

how do you work up a child with GDD

A

routine microarray testing and molecular testing for fragile X

metabolic screening not indicated initially but may consider later

consider REtt syndrome in girls

serum lead if indicated

consider EEG only if sx of epilepsy

if physical findings, use MRI over CT

22
Q

what are the physical features of fragile X

A

prominent forehead
long narrow face
prominent jaw
large ears

23
Q

what is the most common inherited cause of ID

24
Q

what are the most common psychiatric comorbidities in those with fragile X

A

ADHD (80% boys, 30% girls)

anxiety

ASD (30%)

25
what is the most common preventable cause of ID
FASD
26
what are the 3 sentinel facial features of FASD
short palpebral fissure length thin upper lip smooth or flattened philtrum
27
what is the most common genetic disorder
trisomy 21
28
how might an infant with down syndrome look
hypotonia single transverse palmar crease epicanthal folds flat nasal bridge upward slanting palpebral fissures brushfield spots small mouth small ears excessive skin at nape of neck hearing loss, otitis media
29
what medical comorbidities are common with down syndrome
eye disease OSA congenital heart defects thyroid disease neurologic dysfunction GI defects hearing loss
30
what gene is responsible for Prader Willi
deletion on long arm of chr. 15
31
prader willi review
32
what medical condition is common with angelman syndrome (chr. 15 deletion)
90% have epilepsy
33
what are two particular characteristics that may help distinguish those with angelman syndrome
love water/music happy, paroxysmal laugh
34
turner syndrome review
*not an important cause of ID
35
what is a mnemonic to remember the phsycial manifestations of digeorge
CATCH 22 cardiac anomaly T cell deficit cleft palate hypocalcemia (on the 22q11 chromosome)
36
cornelia de lange review
37
which disorder is associated wiht severe self biting
lesch-nyhan syndrome
38
lesch-nyhan review
39
cri du chat review
40
smith-magenis review
moderate MR hyperactivity SEVERE SELF INJURY (head banging, hand biting, pulling out nails)
41
rubenstein taybi review
42
hurler syndrome review
43
PKU review
44
tuberous sclerosis review
45
neurofibromatosis review
46