Paediatric growth and endocrinology Flashcards
what is the shape of a normal growth graph? and what are the 3 main phases?
INFANTILE
CHILDHOOD
PUBERTAL
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what are some methods of measuring?
length
standing and sitting height
head circumference
then plot against norms
how is plotitng of height done? and how are parental heights used?
The mid parental height is calculated in males, by adding 7cm to the mean of parental heights; in females by subtracting 7cm. This gives the height expected at 18 years for the child, and this can be plotted on the percentile chart to predict the child’s height at the appropriate age.
compared against normal percentiles
what imaging is used for measureing growth?
xrays (identifies bone age and conditions such as osteopenia)
what is asked in the hx of a child (in gerneral hx taking)?
birthweight and gestation issues?
PMH
FHX, SHC, schooling
systematic enquiry
dysmorphic assessment
exmaminaitona including pubertal assessment
what are the assessment tools used by a practicioner - give a summary…
- Height/ length/ weight
- Growth Charts and plotting
- MPH and Target centiles
- Growth velocity
- Bone age
- Pubertal assessment
what are the indications for referral in growth disorders?
- Extreme short or tall stature (off centiles)
- Height below target height
- Abnormal height velocity (crossing centiles)
- History of chronic disease
- Obvious dysmorphic syndrome
- Early/late puberty
what are the common categories of short stature?
- Familial
- Constitutional (just naturally small with a delayed bone age, goes through puberty later)
- SGA/IUGR (small for uterine age/ intrauterine growth retardation)
what are some pathalogical causes of short stature?
- Undernutrition
- Chronic illness (JCA, IBD, Coeliac)
- Iatrogenic (steroids)
- Psychological and social
•Hormonal (GHD, hypothyroidism)
•Syndromes (Turner, P-W)
what Ix are done to determine what the cause of short stature is?
FBC and ferritin = General health, coeliac, Chron’s, JCA
U&E, LFT, Ca, CRP = General health, renal and liver disease, disorders of Ca metabolism
Coeliac serology and IgA = Coeliac disease
IGF-1, TFT, Prolactin, Cortisol, (gonadotrophins and sex hormones) = Hormonal disorders
Karyotype = Turner’s syndrome
what is done in a GH stimulation Ix
arginine test
insulin tolerance test
if there is an isolated growth hormone deficiency what is the next ix to be done?
MRI - may show ectopic posterior pit. gland OR small anterior pit. gland.
what is the tx of growth hormone deficiency…pretty obvious
give growth hormone and monitor
what height and weight changes are seen in hypothyroidism?
loss of height and gain in weight
what are the sy/sx of Turners syndrome?
what method is used to stage puberty
Tanner method
- B 1 to 5 (breast development)
- G 1 to 5 (genital development)
- PH 1 to 5 (pubic hair)
- AH 1 to 3 (axillary hair)
- T 2 ml to 20 ml
- SO eg statement as B3 PH3 or G2 PH2 6/6
what is used to measure testicular maturation?
Prader Orchidometer
what age should you worry about early or delayed puberty in boys and girls?
- Boys - early < 9 years (rare), delayed >14 (common, especially CDGP)
- Girl - early <8 years, delayed >13 (rare)
what is constitutional delay of growth and puberty (CDGP)
- Boys mainly
- Family history in dad or brothers (difficult to obtain!)
- Bone age delay
- Need to exclude organic disease
Some other causes of delayed puberty
- Gonadal dysgenesis (Turner 45X, Klinefelter 47XXY)
- Chronic disease (Crohn’s, asthma)
- Impaired HPG axis (septo-optic dysplasia, craniopharyngioma, Kallman’s syndrome)
- Peripheral (cryptorchidism, testicular irradiation)
precocious puberty
Abnormal sex steroid hormone secretion
- Gonadotrophin independent (low/prepubertal levels of LH and FSH)
- Clinical picture: secondary sexual characteristics
Need to exclude Congenital Adrenal Hyperplasia!
Central Precocious Puberty
•Pubertal development
–Breast development in girls
–Testicular enlargement in boys
- Growth spurt
- Advanced bone age
- Need ro exclude a primary lesion - MRI done.
Ambiguous genitalia: Management approach
- Do not guess the sex of the baby!
- Multidisciplinary approach (paed endo, surg, neonatologist, geneticist, psychologist)
- Exam: gonads?/ internal organs
- Karyotype
- Exclude Congenital Adrenal Hyperplasia!- risk of adrenal crisis is first 2 weeks of life
what are the most common causes of acquired hypothyroidism?
autoimmune (hashimotos), fhx, = this will caue childhood issues (lack of height gain, pubertal delay, poor school performance).
what does obese and abnormal mean?
the child is abnormal
what is this?
what does it mean?
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acanthosis nigricans
insulin resistance indicated by this
causes of obesity in childhood?
- SIMPLE OBESITY
- Drugs
- Syndromes - learning difficulties
- Endocrine disorders - growth failure (short, fat)
- Hypothalamic damage - leads to loss of appetite control
what are the symptoms of DM
Sometimes referred to as the 4T’s
Thirsty
Tired
Thinner
Using the Toilet more
DKA symptoms
N and v
Abdo pain
ketotic breath,
drowsiness,
rapid, deep sighig resp - Kausmal Breathing
Coma
Ix done for DM
Finger prick capillary blood glucose test
Result >11mmol/l - Diabetes
Result <11mmol/l - Other cause