S1 Endo Patho Flashcards

1
Q

What are the growth Major problems ?

A
  • Short stature
  • Tall stature
  • Development of secondary sexual characteristics
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2
Q

What are the direct effects of GH ?

A

On liver :

  • glucose syntheses ( gluconeogensis ) and utilization ( for this reason it is increasing during hypoglycemia )
  • RNA synthesis
  • protein synthesis
  • IGF-1

On muscles :

  • Amino acid uptake
  • protein synthesis

On adipose:
Lipolysis ( so in GHD there will be increase in fat deposition )

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3
Q

What are the causes of short stature ?

A
  1. Physiological
    * Constitutional delay
    * Familial short stature
  2. Chromosomal anomalies
    * turner
    * down
  3. GH deficiency
    Children: dwarfism
    Adults : panhypopitutirism
  4. Other diseases
    * primary ( congenital )hypothyroidism
    * congenital heart disease
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4
Q

What are the causes of tall stature ?

A
  1. Physiological
    * Hereditary (2 tall parents)
    * Idiopathic (constitutional)
    * Early development
  2. Chromosomal abnormalities
    * Klinefelter’s syndrome
    * Marfan’s syndrome
  3. GH excess
    * Gigantism (children)
    * Acromegaly (adults)
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5
Q

What are the Investigations of short stature ?

A
  1. Standardized hight charts
  2. GH status
    * random ( baseline) GH > not specific or sensitive
    * dynamic ( stimulation ) GH > by insulin / drugs(clondine-arginine-Ldopa) /exercise/ stress
    * age and gender specific IGF-1 ( used to confirm the diagnosis )
  3. MRI of pituitary
  4. X-ray of the affected bones ( bone age )
  5. Exclude different conditions :
    * systemic diseases
    * congenital heart disease
    * hypothyroidism ( by checking thyroid hormones )
    * chromosomal abnormalities ( down or turner )
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6
Q

What are the Investigations of long stature ?

A
  1. Standardized hight charts
  2. GH status
    * random ( baseline) GH > not specific or sensitive ( if undetectable you can exclude acromegaly/ not necessarily)
    * dynamic ( stimulation ) GH > by OGTT ( GH should normally decrease )
    * age and gender specific IGF-1 ( used to confirm the diagnosis )
  3. MRI of pituitary
  4. Visual field defects
  5. Pituitary hormone secretion decrease , prolactin increase ( in 1/4 of acromegaly cases )
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7
Q

When total pituitary hormone suppression can occur in response to GH ?

A
  1. In GHD
    - specifically in the adults ( panhyopopituitarism )
  2. In excess GH
    - as all hormones will decrease except prolactin
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