Paeds Flashcards

1
Q

Kawasaki

A

Orla ulcers strawberry tongue
Bilat conjunctivitis
Cerv lymphs
Polymorphous rash
fever >5 days

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2
Q

Uti

A

<3 months admit
0-6 months
- atypical features + recurrent USS acutely + dmsa in 6 months
- typical that responds with abx- USS within 6 wks

6 months - 3 yrs old
- atypical acute USS
-recurrent 6wk USS
Both needs dmsa in 6 months

3 yrs+
-atypical USS acutely
- recurrent USS 6 wks + dmsa 6 months

Atypical ft : poor response to abx in 48hrs mass sepsis poor outflow non e coli organism

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3
Q

Gastroenteritis

A

Diarrhoea 5-7 days stops within 2 wks
Vomiting 1-2 days stops within 3 days

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4
Q

Post meningiocococal b infection

A

Audiogram as sensoneural deafness is a complication

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5
Q

newborn with bilateral undescended testes

A

urgent review as associated with congenital adrenal hyperplasia and ambiguous genitalia
if unilateral undescended testes if not descended by 3 months to refer

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6
Q

measles

A

koplik spots - small white spots on bucal mucosa
rash starts behind the ears then to the whole body 0 desquamation that typicalls spares palms and soles
most common complication is otitis media, where complication that causes death is pneumonia
subacute sclerosisng panencephalitis presents 5-10 yrs after disease
kids who come into contact with affected give immunisation w/n 72hrs if not immunised

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7
Q

Roselea infantum

A

Fever followed by rash on trunk
Febrile convulsions common
6 months- 2 yrs old

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8
Q

Phimosis

A

Cannot retract foreskin, ballooning on micturition and no discomfort - reassure and monitor if <2 yrs old
If more than 2 or recurrent uti to refer

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9
Q

Congenital hernias

A

Congenital hernias
inguinal: repair ASAP
umbilical: manage conservatively if not resolved by age 4-5

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10
Q

Scarlet fever

A

Rash usually starts on face then body ‘sandpaper’ pink rash and ‘strawberry’ tongue.

caused by Group A beta-haemolytic streptococcus

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11
Q

Immune thrombocytopenia purpura

A

ITP typically presents in young children with sudden onset of petechiae, bruising, and mucosal bleeding (e.g., nosebleeds). It often follows a viral infection and is characterised by isolated thrombocytopenia on blood tests, with normal white blood cell count and haemoglobin levels.

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12
Q

Cephalohaematoma

A

Several hours after birth, doesn’t cross suture lines, can take months to resolve

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13
Q

Caput succedaneum

A

Forms at birth
Crosses suture line
Resolves after a few days

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14
Q

Acute lymphoblastic anaemia

A

causes pancytopenia but is associated with hepatosplenomegaly, lymphadenopathy, and systemic symptoms such as fever and bone pain,

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15
Q

Factor vII or IX (haemophilia)

A

causes prolonged aPTT due to a coagulation factor deficiency. It is also more likely to present with haemarthrosis (joint bleeding) rather than mucosal bleeding.
X link recessive

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16
Q

Von willebrand

A

Bleeding gums
Most common
Prolonged PT rest normal

17
Q

Developmental milestones motor

A

-7-8months sit without support (refer by 12 months)
-12 months cruises
-13-15months (refer at 18 boys and 24 months girls) walks without support
-2 yrs runs (refer by 2.5 yrs)
-3yrs bike and walk up stairs
-4 yrs hop on one leg

18
Q

No school exclusion

A

Conjunctivitis
Fifth disease (slapped cheek)
Roseola
Infectious mononucleosis
Head lice
Threadworms
Hand, foot and mouth

19
Q

immunization schedule

A

2 months - 6 in 1 (diptheria, hep B, pertussos, polio, hib, tetanus), rotavirus, Men B
3 months - 6 in 1, rotavirus, PCV
4 months - 6 in 1, Men B
12 months - MMR, PCV, HIb/Men C, Men B
3-4 yrs - 4 in 1 and tetanus
12-13 yrs - HPV and Men ACWY

20
Q

Gillick competence

A

right to accept treatment not to refuse treatment

Fraser guidelines only for contraception

21
Q

sturge weber syndrome

A

learning disability with epilepsy

22
Q

prader willi

A

genital hypoplasia, obese baby, learning disability, neonatal hypotonia, small or non palpable testes

23
Q

fragile X

A

X-linked
learning disability
large head
hyperactivity
autism

24
Q

patent ductus ateriosus

A

contunuous machine like murmur maximally heard under the L clavicle
common in premature babies

25
Q

Klinefelters 47 XXY

A

High LH low testosterone
Gynaecomastia, small testes, tall

26
Q

One hand dominance

A

if less than 18 months old then refer as may be a sign of hemiparesis or cerebral palsy

27
Q

DUchenne muscular dystrophy

A

leardning difficulties
mobility issues + gowers sign

28
Q

jaundice

A

less than 24hrs post birth - rhesus imcompatibility
after 24hrs is physiological or breast feeding jaundice
after 3 wks is biliary atresia or hypothyroisidm

29
Q

noonans syndrome

A

pectus excavatum, webbed neck, pulmonary stenosis

30
Q

downs syndrome + turners

A

monitor TFTs

31
Q

edwards trisomy 18

A

micrognathia, low set ears, rocker bottom feet, overlapping fingers

32
Q

patau trisomy 13

A

polydactyly
microcephaly scalp lesions

33
Q

pierre robinson

A

posterior displacement of the tongue
cleft palate

34
Q

williams syndrome

A

friendly outgoing personality, short stature, supravalvular aortic stenosis, LD

34
Q

learning disability

A

downs
cri du chat
williams syndrome
fragile X

35
Q

turners (45X)

A

short stature, webbed neck, primary amenorrhoea, horse shoe kidney, bicuspic aortic valve, coarctation of the aorta, high arched palate

36
Q

nuchal scanning - cause inc nuchal translucency

A

Down’s syndrome
congenital heart defects
abdominal wall defects

37
Q

Causes of hyperechogenic bowel on nuchal scan

A

CMV, CF, downs