Peds Flashcards
Normal Pubertal development in female. the sequence?
- breast budding (thelarche) 2. axilary hair, body odor, mild acne (pubarche) 3. growth spurt 4. menarch
Normal Pubertal development in male. the sequence?
- testicular enlargement 2. penile enlargement 3. axilary hair, body odor, mild acne (pubarche) 4. growth spurt
ambiguous genitalia. workup?
- chromosome analysis
- pelvic ultrasonogram ifMullerian structures are present (uterus)
- if gonads palpable
- testosterone and dihydrotestosterone (DHT) ratio
- LH and FSH
- hCG stimulation test
if gonads not palpable (most likely congenital adrenal hyperplasia due to 21 hydroxylase deficiency)
- 17-hydroxyprogesterone
- serum electroytes
- plasma renin activity
Community acquired pneumonia in children.
Abx?
Abx for severe pneumonia?
what defines severe pneumonia?
- Amoxicillin 30mg/kg TDS 3-5 days
- severe pneumonia means one of following
- severe respiratory distress
- severe hypoxia or cyanosis
- marked tachycardia
- altered mental state
- empyema
- children with severe pneumonia require ICU admission and
Ceftriaxone 50mg/kg IV daily
AND
Flucloxacillin 50mg/kg IV 6 hourly
(consider azithromycin if pneumonia progresses)
down-slanting papebral fissure, wide spread eyes, low set ears, +- ptosis
Dx? etiology?
what other features?

Noonan’s syndrome
chromosome 11 autosomal dominant mutation
short stature
pulmonary valve stenosis
webbed neck
failure to thrive, mild
abnormal cardiac rhythm,
intellectual disability
a toddler with jaundice, lethargy, splenomegaly
Hx of neonatal jauntice, Family Hx of gall stones
Dx and blood film?
hereditary spherocytosis
- microsphercytes on blood flim
- autosomal dominant
HCV + mother,
what to do with the baby?
breast feeding ?
HCV-PCR at 2-6months
anti-HCV at 18-24 months
breastfeeding ok except in the presense of cracked or bleeding nipples
croup Tx? Management?
- dexamethasone 0.6mg/kg for all.
- mild, consider sending home
moderate, observe four 4 hours
severe, add nebulized epinephrine, oxygen, observe 4 hours. If not improved, consider hospitalization.
the pattern of inheritance for
Huntington’s disease
cystic fibrosis
G6PD deficiency
Thalassemia
hemochromatosis
hereditary hemorrhagic telangiectasia
Huntington’s disease : autosomal dominant
cystic fibrosis : autosomal recessive
G6PD deficiency : X-linked recessive
Thalassemia :autosomal recessive
hemochromatosis : autosomal recessive
hereditary hemorrhagic telangiectasia : autosomal dominant
sore throut 3 weeks ago,
polyarthralgia
fever
Dx? and Management?

acute rheumatic fever
admission. confrim Dx with throat swab
Tx with PO penicillin V or amoxicillin for 10 days, NSAIDS,
IM benzathine penicillin for secondary prevention.
echocardiography
pertussis
exclusion from school? how long?
- 21 days from the onset of any cough (catarrhal period)
- 14 days from the onset of paroxysmal cough
- 5 days after starting appropriate antibiotics.
congenital infections that affect the fetus or infant?
TORCH (Toxoplasma, others, rubella, CMV, HSV)
others include parvoB19, enterovirus, VZV, coxackie, listeriosis, syphilis
5 months old, runny nose, fever 40 C for the past two days, otherwise active and healthy.
Temperature dropped normal and maculopaular rash on trunk.
Dx?

roseola infantum
a toddler with lethargy and inactivity,
a fundoscopic exam shows a macular cherry spot.
Dx ? etiologu?
Tay -Sachs syndrome
autosomal recessive
deficiency in beta hexosaminadase A
a toddler with
anemia, leukopenia, bone pain, enlarged spleen, thrombocytopenia
+
loss of muscle tone, loss of motor skills, muscle spasm, trouble swallowing
Gaucher disease
autosomal recessive
glucocerebrosidase deficienty
lysosomal disease
8 month
a history of sudden bending the trunk and flexion of upper limbs.
episodes happen in a cluster.
Dx and Tx?
Infantile spasm
Tx : steroid, ACTH, vigabatrin
pediatric
hypoglycemia Tx
2ml/kg 10% dextrose IV
regular, monomorphic wide QRS tachycardia in children
V/S stable.
Tx?
ADENOSINE!!!!
such tachycardia in children are often SVT with abberancy, hence responsive to adenosine.
if adenosin doesn’t work,
consider VT and amiodarone
congenital rubella syndrome
the triad of manifestations
microcephaly
PDA
cataract