Disclaimer
We’re actively expanding Guideline Genius to cover the full UKMLA content map. You may notice some conditions not uploaded yet, or articles that only include diagnosis and management for now. For updates, follow us on Instagram @guidelinegenius.
We openly welcome any feedback or suggestions through the anonymous feedback box at the bottom of every article and we’ll do our best to respond promptly.

Thank you for your support.
The Guideline Genius Team

Total Live Articles: 312

Osteomalacia and Rickets

Definition

Osteomalacia: defective mineralisation of existing bone matrix (osteoid) in adults or children.

Rickets: defective mineralisation of newly formed bone at the growth plate in children before growth plate closure.

Aetiology

Aetiology of osteomalacia and rickets is largely the same.

Most common: vitamin D deficiency [Ref]

Rarer causes: [Ref]

  • Disorders of vitamin D metabolism (e.g. 1 alpha-hydroxylase deficiency, vitamin D receptor mutation)
  • Disorders of phosphate metabolism (e.g. X-linked hypophosphataemia – due to increased FGF23 activity)

Clinical Features

Osteomalacia and rickets have distinctive clinical presentations.

Osteomalacia

Can occur in both adults and children

Main features: [Ref1][Ref2]

  • Bone pain and tenderness (tend to be diffuse)
  • Proximal myopathy
  • Difficulty walking
    • Waddling gait
    • Increased risk of falls

 

  • Severe diseases
    • Pathological fractures
    • Bone deformity (e.g. bowing of lower limbs)

Rickets

Only occurs in children (before growth plates have fused)

Main features: [Ref1][Ref2]

  • Impaired growth – not always present
    • Short stature
    • Delayed walking
  • Bone defomirties
    • Bowing of the legs
    • Genu varum (more common than genu valgum)
    • Swelling of the wrists, knees, and ankles (from bone-cartilage junction distension)
  • Harrison groove – horizontal depression on the lower edge of the chest (at the attachment point of the diaphragm)

Neonatal presentation: [Ref]

  • Late closing of fontanelles and soft skull (craniotabes)
  • Poor feeding
  • Irritability
  • Hypocalcaemic seizures

Investigation and Diagnosis

Blood Tests

Typical biochemical changes (for both osteomalacia and rickets): [Ref1][Ref2]

  • ↑ PTH
  • ↑ ALP
  • ↓ 25-hydroxyvitamin D
  • ↓ Calcium ↓ Phosphate (but maybe normal in early disease / mild disease)

Be aware that the test of choice for vitamin D deficiency is serum 25-hydroxyvitamin D​​​​​​, the major circulating form of vitamin D.

Imaging

Typical imaging findings for osteomalacia[Ref1][Ref2]

  • Looser zones (pseudofractures)
  • Cortical thinning
  • Diffuse osteopaenia (bone appears less dense)
  • Pathological fractures possible

Typical imaging findings for rickets[Ref1][Ref2]

  • Growth plate (metaphyseal) abnormalities
    • Widening
    • Cupping
    • Irregularity
  • Bone deformities
    • Bowing of legs
    • Genu varum (more common than genu valgum)

Management

For nutritional deficiency osteomalacia / rickets → ensure adequate vitamin D and calcium [Ref1][Ref2]

  • Age-appropriate dose of vitamin D
  • Ensure adequate dietary calcium intake
    • Give supplementation if insufficient

Notes on various types of vitamin D and their use:

Vitamin D type Description Indication
 

Native forms of vitamin D

  • Preferred: Vitamin D3 (cholecalciferol)
  • Alternative: Vitamin D2  (ergocalciferol)
 

Must be hydroxylated in the liver to 25-hydroxyvitamin D (calcifediol), then in the kidney into 1,25-dihydroxyvitamin D (calcitriol) for biological activity

  • Routine vitamin D deficiency
  • Osteoporosis
  • Supplementation in the general population
25-hydroxyvitamin D (calcifediol) Major circulating form of vitamin D (produced by 25-hydroxylation in the liver)

(If vitamin D deficiency is suspected, 25-hydroxyvitamin D is measured)

  • Considered in liver impairment (calcifediol does not require hepatic hydroxylation, it can be readily hydroxylated by the kidneys)
Activated vitamin D metabolites (bypassing the renal activation process)
  • 1-α-hydroxycholecalciferol (alfacalcidol)
  • 1,25-hydroxyvitamin D (calcitriol)

 

Both alfacalcidol / calcitriol can be given as supplements to bypass the renal activation process (thus considered activated vitamin D metabolites):
  • Calcitriol is the fully active form of vitamin D (produced naturally by the kidney’s 1-alpha hydroxylase)
  • Alfacalcidol is synthetic, and it requires liver activation to be fully active

 

Impaired renal 1-alpha hydroxylase activity:
  • Stage 4/5 CKD (specific indication in CKD article)
  • Hypoparathyroidism 

Not used for routine deficiency replacement or for general population supplementation due to increased risk of hypercalcaemia

Share Your Feedback Below

UK medical guidelines made easy. From guidelines to genius in minutes!

Quick Links

Cookie Policy

Social Media

© 2026 GUIDELINE GENIUS LTD