Bone Flashcards

(16 cards)

1
Q

what does PTH do?

A

increases CA
(dec in PO4)

  • releases Ca from bone
  • inc Ca absorp from gut
  • inc Ca uptake from kidneys
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2
Q

what is the work up for short stature

A
cbc
liver and renal panel
ESR?CRP for implammatory
TTG to rule out celiac
TSH/FT4 
carotene and folate for nutrition
Ca/mg/PO4
Urine - RTA
Bone age
Karyotype for a girl

(IGF 1/IGF BP3
porlactin)

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3
Q

what are the CF of hypocalcemia

A

asymptomatic
msl: intermittent muscle cramps - at rest or during exercise, laryngospasm, tetany
CNS: SZ, papillodema, basal ganglia calcifcation
H&N: cataract, enamel hypoplasia
CVS: QTc and ST prolongation, arrythmia, HB

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4
Q

what are common causes of Vit D def

A
Lack of dietary intake
Lack of sun exposure
liver disease
renal disease
drugs - phenytoin. phenobar
Vit D resistance
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5
Q

what are the 4 main causes of hypocalcemia

A
  1. Vit D def
  2. Malabsorption
  3. hypoparathyroidism - congenital or acquired
  4. pseudohypoparathyroidism - resistance to PTH
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6
Q

if pt has hypopartathyroidism, what will the PTH, Calcitriol, Ca and PO4 be

A

low PTH
low calcitriol
low Ca
high PO4

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7
Q

what are risk factors for Vit D def

A
exclusive BF
mothers that are Vit def
darker skin
poor sun exposure
northern communities
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8
Q

what are the 2 main groups of rickets?

A

hypocalcemic

hypophosphatemic

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9
Q

what are hypophosphatemic causes of rickets?

A

1) not enough PO4 going in: malnutrition, GI losses, antacids
2) too much out - congenital disorders, systemic illness

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10
Q

what are clinical features of rickets in the newborn

A

FTT
poor energy
muscle weakness
bone deformities and fractures

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11
Q

what are clinical features of Rickets

A
frontal bossing
craniotabes
delayed closure of fontanelles
rachitic rosaries
Harrison Groove
enlarged wrists and ankles
bowing
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12
Q

what are radiologic features of rickets

A

widening of distal ulna and radius
concave cupping
frayed and poorly demarcated ends
increased space of writs

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13
Q

what are the lab abnormalities of Vit D def

A
Vit D low
Low/N Ca
Low PO4
high PTH
high ALP
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14
Q

what is Albright hereditary osteodystrophy

A

pseudohypoparathyroidism - resistance to PTH
High PTH but LOW Ca

short stature, round facies with a low nasal bridge, obesity, disproportionate shortening of the limbs (particularly brachydactyly of the third, fourth, and fifth metacarpals and first distal phalanx), heterotopic ossification, and intellectual disability.

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15
Q

what are causes of early and late neonatal hypocalcemia?

A

Early - (birth to 4 days) = prematurity, maternal diabetes, perinatal asphyxia, and IUGR
Late - (5 to 10 days) = hyperphosphatemia, hypomagnesaemia, hypoparathyroidism, maternal vit D deficiency, and infantile osteopetrosis.

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16
Q

patient is seen for bowing of the legs.

BW phosphorus level is very low, but the PTH level is normal. Dx

A

X-linked hypophosphatemic rickets