Paediatrics 👧🏾 Flashcards

1
Q

Speech sound disorder

A

Dysfunctional speech articulation presenting as difficulty articulating specific sounds

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2
Q

Child hood onset fluency disorder

A

Dysfunction in speech fluency (stuttering

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3
Q

Social communication disorder

A

Dysfunctional verbal and non-verbal communication. Unlike autism, these patients don’t have restricted interests or repetitive behaviours

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4
Q

When does the Babinski reflex naturally disappear

A

One year old

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5
Q

Constitutional growth delay

A

 Growth curve remains consistent, but is low. In essence it’s lagging behind the other children. NBME case. Has delayed bone age . Children will eventually reach a good height

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6
Q

Familial short stature

A

 Short stature, with at least one of the parents also being short. Burnage corresponds with chronological age, puberty is not delayed. Adult height will remain low

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7
Q

Main differences between constitutional gross delay and familall short stature

A

Constitutional growth delay patients have a delayed bone age, and will eventually achieve target height. FSS will have normal bone age and won’t reach target height

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8
Q

On growth chart, if a patient is falling off the growth chart (crossing two major percentile lines) what does that indicate

A

Failure to thrive. Not familial short stature of constitutional growth delay

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9
Q

Infants with failure to thrive will fall off the curves in which order

A

Wait, height, heads Circumference 

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10
Q

Newborns lose what percent of the body weight at birth, they should regain it by how long

A

10%, then by two weeks

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11
Q

Order this for female development:

Thelarche, menarche, growth spurt, pubarche

A

Thelarche, pubarche, growth spurt, menarche

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12
Q

Order this for male development:

Gonadarche, growth spurt, pubarche, Adrenarche

A

Gonadarche, pubarche, adrenarche, growth spurt

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13
Q

Androgen insensitivity patience. What procedure must be done

A

Removal of the gonads to prevent cancer

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14
Q

Horseshoe kidney seen in which trisomy

A

 Edward

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15
Q

Meckel diverticulum scene in which trisomy

A

Edward

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16
Q

Which trisomy does holoprosencephaly belong to

A

patau

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17
Q

Which trisomy does omphalocele belong to

A

Patau

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18
Q

Polydactyl is seen in which trisomy

A

Patau

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19
Q

Lymphedema in neonate can be seen in which chromosome issue

A

Turners

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20
Q

If untreated Fabry. Increase risk of what

A

Thromboembolism

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21
Q

Tay Sachs vs Neimann pick

A

HSmeg in Pick

22
Q

Main symptoms of meta chromatic leukod

A

Ataxia and dementia

23
Q

Exaggerated startle response

24
Q

Hereditary fructose intol

A

Aldolase def.
Hypoglycaemia, Jaundice, cirrhosis, vomiting. After eating fruit juice or honey. Lactic acidosis. Urine dipstick is negative

25
Main cause of failure to thrive in cystic fibrosis
Pancreatic insufficiency
26
APGAR
Activity (active 2, only flex 1, absent 0), pulse (>100 2, <100 1, absent 0), grimace (active 2, some flexion 1, flaccid 0), appearance (pink 2, blue extrem 1, blue all over 0), respiratory (vigorous 2, slow irreg 1, absent 0). 8-10 good 4-7 observe 0-4 resus
27
CHARGE
Coloboma, heart disease, atresia of the choanae, retarded, genital hyperplasia, ear abnormality
28
VACTERL syndrome
Vertebral, Anal, cardiac, TE, Renal, limb
29
Gastroschisis is associated with what amniotic fluid issue
Oligohydramnios. Also elevated AFP
30
Omphalocele versus gastroschisisl. Which is associated with trisomies and Beckwith Witteman. Which is associated with oligo and which is associated with polyhydramnios
Gastroschisis is not associated with other syndromes. And is associated with oligohydramnios. Vice versa for omphalocele
31
Alagille syndrome
Too few bile ducts for adequate drainage. Causes CHOLESTASIS
32
Jaundiced neonate, who is febrile, hypertensive and tachypnoeic needs what
Sepsis work up an ICU monitoring
33
Lecithin : sphingoM ???
>2, good to go. Mature fetal lungs.
34
Diagnose this neonatal rash: Onset within three days. Red pustules on the trunk and proximal extremities. Resolves in a week
Erythema toxicum neonatorum
35
Diagnose this neonatal rash: Present at birth. White, firm papules on the face. Resolves in a month
Millia
36
Diagnose this neonatal rash: Not present at birth. History of overheating. Erythematous papules in areas of occluded eccrine sweat gland
Milia rubra. Can you give topical corticosteroids it’s
37
Diagnose this neonatal rash: Present at birth. Diffuse non-read pustules. Eventually becoming hyperpigmented macules with a scale
Neonatal pustular melanosis
38
Diagnose this neonatal rash: Onset around three weeks. Red papules and pustules only on the face and scalp
Neonatal Cephalic pustulosis (neonatal acne)
39
When does neonatal abstinence syndrome kick in
Over 24 hours after birth, when the mothers circulatory drug load decreases in the baby
40
ALL symptoms gradual or abrupt
Abrupt
41
AML vs ALL. Which in blocks and which in whites
AML in blocks ALL in whites more
42
Second most common place to get neuroblastoma
Paraspinal symp chain
43
Neuroblastoma: does it doesn’t have opportunity to cross midline
Can cross
44
Some more random signs of Neuroblastoma
Abdominal distension. Horners if cervicle Symp chain. Opsiclonus myoclonus. Cord compression if paraspinal. FTT, anemia and fever are rare
45
WAGR syndrome
Wilms , aniridia , genital issues, retardation
46
Horshoe kidney is associated with m which renal CA
Wilms
47
Wilms vs Neuroblastoma
Wilms is smooth, stays on one side. 3-5 years old usually. NeuroB usually 2 or less years old. Can cross midline. Irregular and crosses midline more
48
Ewing’s translocation
11:22
49
Ewing’s vs osteosarcoma. Which has systemic symptoms more
Ewings
50
Ewing’s found where in long bones
Diaphysis
51
Single lesion of langerhan cell histeocytosis… Tx?
Sx resection