paeds Flashcards
unable to palpate testes, normal penis with no hypospadias anus is patent
normal baby. what do you need to rule out?
21-hydroxylase deficiency. These infants
may present with ambiguous genitalia or bilateral undescended testicles
and are at risk of a salt-losing adrenal crisis (vomiting, weight loss,
floppy unwell infant), typically around 1–3 weeks of age. It is therefore
important to measure urea and electrolytes in addition to chromosomal analysis and a pelvic ultrasound to look for the location of the sex
organs.
status 2 doses of benzo weened off phenytoin recently what next?
IV phenytoin as 2 doses benzo and no longer on pheyntoin
iron overdose presentaiton
2 phases
vomitting diarrhoea gastric irritation + malaena
>24h improvement then deterioraiton with liver failure drowsiness andcoma
neonate with recurrant ecoli. uti/sepsis, vomitting catarcts
Galactosaemia
Phenylketonuria
PKU is an autosomal recessive metabolic condition resulting in a defect
in enzyme phenylalanine hydroxylase, which converts phenylalanine to
tyrosine. Due to the accumulation of phenylalanine and conversion to
phenylketones, unrecognized and untreated PKU can result in seizures
and musty smelling urine and eventually microcephaly and learning
difficulties.
CAH management
IV dextrose IV hydrocortisone and 0.9% saline
neonate with jaundice after 2 weeks from day 5, pale stool dark urine
biliary atresia must be investigated due to risk of cirrhosis
preterm on itu recieving formula milk, billious aspirates from ng, distended abdomen bloody stool, NEC
NBM, IV fluids AXR, surgical review
VACTERL
vertebral, anal imperforation, cardiac, tracheo-oesophageal fistula, renal limb anomalies
symmetrical vs asymetrical IUGR
symmetrical - smoking, alcohol, congenital infection
asymmetrical - maternal diabetes preeclampsia –> placental insufficiency
intersusseption management in DGH
Up to 75 per cent of cases may be reduced by air insufflation rectally,
but if this fails the child will need to be taken directly to theatre as there
is a risk of perforation with the procedure. As it is unlikely that a district
general hospital will be able to take such a young child to theatre, all
procedures should be carried out in a paediatric surgical centre
CMV infection which is not deafness iugr hydrocephalus thrombocytopaenia congenital cardiac
congenital cardiac not associated
SCID B CELLS T CELLS AND iG
LOW B LOW T LOW IG
wiskott aldrich W A T E R
WASP GENE APC'S thrombotcytopaenia eczema recurrant infection
A 3-year-old child presents to the GP with a chronic cough for the last month.
He had previously been fit and well since he suffered a severe pertussis infection
when he was 1 month of age. He has subsequently been fully immunized but
was noted to be on the 0.4th centile for height. What is the most likely cause
for his cough?
severe respiratory infection in early childhood can present later in
life with bronchiectasis. caused by dilatation and poor mucociliary
clearance, predisposing to further infection. Any chronic illness may
impact on the growth and development of a child.
children aged above 5 most common pneumonia?
mycoplasma
strep is less than 4