Endoctine Flashcards
Which infants and children are at higher risk of hypoglycaemia
Premature
IUGR or small for gestational age
Born to diabetic mothers
Septic or severe illness
What is the standard value of hypoglycaemia in paediatric
<2.6 glucose
Symptoms of hypoglycemia
Poor feeding
Lethargy
Seizures
Coma
Older: anxiety, palpitations, tremors, blurred vision, confusion and weakness.
What are the causes of hypoglycaemia in paeds
Hyperinsulinism
Counter-regulatory hormone deficiency (GH deficiency, hypocortisol, glucagon deficiency)
Glycogen storage or release diseases
Mt fatty acid oxidation defects
Keton utilisation defects
Defective gkuconeogenesis
Exogenous drugs
Miscellaneous causes (ketotic, hypoglycaemia, reactive hypoglycaemia)
Treatment of congenital hyperinsulinism
Diazoxide
Best managed in tertiary as some need surgery
what is the average rate of growth in the first 2 years of life
25cm per year in the first year then 12 cm per year in the second .
what regulates growth in the pubertal period
GH and sex steroids (oestrogen and teestosterone)
What is the average height difference between girls and boys during puberty
13cm
what is the cut off age foe measuring a child with a infantometer
2 years, then use a stadiometer
what is the normal mid parenteral height
indicates a child’s genetic growth potential
average of parents height and add or subtract 6.5 for boys or girls respectively. If above 8.5 cm outside target height investigate further
what are the clinical clues to the presence of endocrine cause of short statue
- GH deficiency- Cherubic appearance face (noncancerous painless growths in child’d jaw, lwading to wide jaw and round cheeks)
- Increased weight to height ratio, child appears obese
(Clues: hypoglycemia and micropenis)
list the endocrine causes of short statue
Hypopituitarism
GH deficiency
Hypothyroidism
precocious puberty
CAH
Cushings syndrome
Pseudohypoparathyroidism
Poorly controlled DM
causes of pituitary gland malformations
Congenital
Cranial malformations: Holoprosencephaly, Septo-optic dysplasia and midline craniocerebral
Embryonic defects: Pituitary hypoplasia, Pituitary aplasia, Congenital absence of pituitary gland
Acquired: Tumours, Cranial radiotherapy or surgery, head trauma, Infection from meningitis/encephalitis, Infiltrative disorders ei Langerhans cell histiocytosis&sarcoidosis
Investigations for suspected hypopituitarism
Thyroid function
Serum cortisol
IGF
CAuses of tall statue
Thyrotoxicosis
Precocious Puberty
CAH
Gigantism
Genetics (Marfans, Klinefelter, Soto syndrome & homocystinuria )