Osteomalacia and Rickets Flashcards

1
Q

Define Osteomalacia:

A

Disorder of mineralisation of the bine matrix (there is a normal amount of bone just lack of mineralisation)

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2
Q

Define Rickets:

A

Disorder of defective mineralisation of cartilage in epiphyseal growth plates in CHILDREN.

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3
Q

Aetiology/risk factors:

A

Decreased Vitamin D exposure:

  • low sunlight exposuree
  • Low dietary deficiency
  • reduced 25-hydroxylation - liver disease or drugs
  • reduced 1a-hydroxylation due to chronic renal failure or hypoparathyroidism.

Vitamin D resistance:

  • Renal osteodystrophy
  • Anti-convulsants (induce liver enzymes that break down the 25-hydroxyVit D
  • Renal phospahte wasting
  • Faconi’s
  • Renal tubuar acidosis
  • Hereditary Rickets
  • tumour induced
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4
Q

Faconi’s syndromes triad:

A
  • Phosphaturia
  • Glycosuria
  • Amino aciduria

GAP

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5
Q

Epidemiology:

A

More common in women

More common in industralised countries

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6
Q

Symptoms of Osteomalacia:

A
Bone pain 
Fractures esp around the femoral head 
Proximal myopathy 
Weakness 
Malaise
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7
Q

Symptoms of Rickets:

A
Knocked knees
Bow legged 
Hypotonia 
Growth retardation 
Skeletal deformities
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8
Q

Signs of osteomalacia:

A
Bone tenderness
Proximal muscle weakness
Waddling gait 
Trousseau's sign 
Chvostek's sign
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9
Q

Signs of rickets:

A

Bossing of frontal and pariatel

Costochondral swelling (rickety rosary)

Knock Knees

Short stature

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10
Q

Investigations:

A
Bloods:
Low or normal Calcium 
Low 25-hydroxy vit D
High ALP
Low phosphate 
High PTH (secondary hyperparathyroidism)
U+Es
ABG (renal tubular acidosis)

Radiography:

  • Looser’s Zone (pseufractures)
  • Osteopenia

Bone biopsy after double tetracycline labelling

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11
Q

Management:

A

Vitamin D or calcium supplements

If malabsorption or liver failure give ergocalciferol (vitamin D2)

If renal disease or vitamin D resistance give alfacalcidiol or calcitriol (vitamin D3)

24hr urinary and plasma calcium

Treat the cause

Monitor:
o	Serum calcium 
o	Phosphate 
o	ALP
o	PTH 
o	Vitamin D
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12
Q

Complications:

A

Hypocalacemia - seizures and tetany

Bone deformities

Cardiac arrhythmia

Depression

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13
Q

Prognosis;

A

With treatment the radiological appearance and symptoms will improve.

Bone are likely to be permanent.

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