Paediatric growth and endocrinology Flashcards

1
Q

what is the shape of a normal growth graph? and what are the 3 main phases?

A

INFANTILE

CHILDHOOD

PUBERTAL

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2
Q

what are some methods of measuring?

A

length

standing and sitting height

head circumference

then plot against norms

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3
Q

how is plotitng of height done? and how are parental heights used?

A

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

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4
Q

what imaging is used for measureing growth?

A

xrays (identifies bone age and conditions such as osteopenia)

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5
Q

what is asked in the hx of a child (in gerneral hx taking)?

A

birthweight and gestation issues?

PMH

FHX, SHC, schooling

systematic enquiry

dysmorphic assessment

exmaminaitona including pubertal assessment

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6
Q

what are the assessment tools used by a practicioner - give a summary…

A
  • Height/ length/ weight
  • Growth Charts and plotting
  • MPH and Target centiles
  • Growth velocity
  • Bone age
  • Pubertal assessment
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7
Q

what are the indications for referral in growth disorders?

A
  • 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
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8
Q

what are the common categories of short stature?

A
  • Familial
  • Constitutional (just naturally small with a delayed bone age, goes through puberty later)
  • SGA/IUGR (small for uterine age/ intrauterine growth retardation)
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9
Q

what are some pathalogical causes of short stature?

A
  • Undernutrition
  • Chronic illness (JCA, IBD, Coeliac)
  • Iatrogenic (steroids)
  • Psychological and social

•Hormonal (GHD, hypothyroidism)

•Syndromes (Turner, P-W)

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10
Q

what Ix are done to determine what the cause of short stature is?

A

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

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11
Q

what is done in a GH stimulation Ix

A

arginine test

insulin tolerance test

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12
Q

if there is an isolated growth hormone deficiency what is the next ix to be done?

A

MRI - may show ectopic posterior pit. gland OR small anterior pit. gland.

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13
Q

what is the tx of growth hormone deficiency…pretty obvious

A

give growth hormone and monitor

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14
Q

what height and weight changes are seen in hypothyroidism?

A

loss of height and gain in weight

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15
Q

what are the sy/sx of Turners syndrome?

A
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16
Q

what method is used to stage puberty

A

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
17
Q

what is used to measure testicular maturation?

A

Prader Orchidometer

18
Q

what age should you worry about early or delayed puberty in boys and girls?

A
  • Boys - early < 9 years (rare), delayed >14 (common, especially CDGP)
  • Girl - early <8 years, delayed >13 (rare)
19
Q

what is constitutional delay of growth and puberty (CDGP)

A
  • Boys mainly
  • Family history in dad or brothers (difficult to obtain!)
  • Bone age delay
  • Need to exclude organic disease
20
Q

Some other causes of delayed puberty

A
  • 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)
21
Q

precocious puberty

A

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!

22
Q

Central Precocious Puberty

A

•Pubertal development

–Breast development in girls

–Testicular enlargement in boys

  • Growth spurt
  • Advanced bone age
  • Need ro exclude a primary lesion - MRI done.
23
Q

Ambiguous genitalia: Management approach

A
  • 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
24
Q

what are the most common causes of acquired hypothyroidism?

A

autoimmune (hashimotos), fhx, = this will caue childhood issues (lack of height gain, pubertal delay, poor school performance).

25
Q

what does obese and abnormal mean?

A

the child is abnormal

26
Q

what is this?

what does it mean?

A

acanthosis nigricans

insulin resistance indicated by this

27
Q

causes of obesity in childhood?

A
  • SIMPLE OBESITY
  • Drugs
  • Syndromes - learning difficulties
  • Endocrine disorders - growth failure (short, fat)
  • Hypothalamic damage - leads to loss of appetite control
28
Q

what are the symptoms of DM

A

Sometimes referred to as the 4T’s

Thirsty

Tired

Thinner

Using the Toilet more

29
Q

DKA symptoms

A

N and v

Abdo pain

ketotic breath,

drowsiness,

rapid, deep sighig resp - Kausmal Breathing

Coma

30
Q

Ix done for DM

A

Finger prick capillary blood glucose test

Result >11mmol/l - Diabetes

Result <11mmol/l - Other cause