11.2 Growth Disorders Flashcards

1
Q

baseline Ix for short stature?

A
  • skeletal bone age (left hand and wrist)
  • karyotype
  • systemic screen: FBE, ESR, UEC, LFT, TFT, Ca, Phos, coeliac, urine MCS, IGF-1
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2
Q

biochemical dx of growth deficiency?

A

peak (after stimulation) of <10mU/L

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3
Q

how tall in untreated GH deficiency?

A

males 140cm

Females 130cm

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4
Q

when to refer/investigate height for severe?

A
  • more than 3SD below mean
  • more than 6cm below 3rd centile
  • positive screening tests
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5
Q

when to refer for less severe growth ?

A

is height is 2-3 SD below or under 3rd centile

  • systemic screen-NAD
  • observe for 6/12 months
  • if growth rate <25p refer
  • if >25p, monitor
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6
Q

Bone age useful how?

A
  • severity of growth problem
  • remaining growth potential
  • height prognosis
  • estimated adult height calculation
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7
Q

eligibility criteria in australia?

A

-<1st percentile
-biochem growth hormone deficiency
-

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8
Q

bone ages that will exclude growth hormone use?

A

girls: 13.5

boys 15.5

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9
Q

any girl with unexplained short stature, no signs…. should consider?

A
  • turner syndrome
  • do a karyotype
  • can end up 20cm shorter
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10
Q

Turner Syndrome at diagnosis investigations:

A
  • ECG, cardiac, ECHO, cardiac/aortic arch/MRI
  • audiology
  • risk for diabetes
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11
Q

what to watch out for in Turner’s Syndrome to investigate and monitor?

A

Cardiovascular malformations

-ECHOs

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12
Q

management of turner syndrome?

A
  • GH as soon as possible
  • pubertal induction
  • maintain Ca intake
  • audiology, ECHO
  • transition to young adult clinic
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13
Q

puberty correlate better with what measurement?

A

bone age

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14
Q

basic screens for tall stature?

A
  • bone age
  • karyotype
  • IGF-a, random GH
  • TFT
  • urine
  • echo
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15
Q

options for height limitation?

A
  • avoid if possible
  • high dose testosterone
  • high dose oestrogen
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