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Rickets

from Section I - Musculoskeletal radiology

Published online by Cambridge University Press:  22 August 2009

James R. D. Murray
Affiliation:
Bath Royal United Hospital
Erskine J. Holmes
Affiliation:
Royal Berkshire Hospital
Rakesh R. Misra
Affiliation:
Buckinghamshire Hospitals NHS Trust
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Summary

Characteristics

  • Rickets is inadequate mineralisation of osteoid in the immature skeleton.

  • Osteomalacia (softened bone) is the same inadequate mineralisation of bone, but occurring in the adult skeleton without the growth disturbances of rickets.

  • Rickets occurs secondary to vitamin D deficiency/dysfunction, and with inadequate intake of calcium and phosphorus.

  • Associated with sunlight deficiency, renal disease, liver disease and malabsorption, because of the effect on vitamin D synthesis.

Clinical features

  • Infants may present with convulsions, tetany or failure to thrive.

  • Craniotabes (skull deformity) develops early.

  • Muscular hypotonia is common.

  • Wrist, ankle and knee swelling.

  • ‘Rickety rosary’ – costochondral junction enlargement.

  • Harrison's sulci – lateral chest-wall gutters secondary to muscular action on weakened ribs.

  • Leg bowing and knock-knees become more prominent on weight bearing.

  • Spinal involvement and long-bone fractures are late manifestations.

Radiological features

  • Metaphyses of long bones subjected to stress are particularly involved (wrists, ankles, knees).

  • Irregular widened epiphyseal plates – due of the failure of mineralisation.

  • Cupping and fraying of metaphyses – best seen where growth is maximal.

  • Coarse trabecular pattern.

  • Long-bone bowing.

  • Periosteal reaction may be present.

Management

  • Identify and treat underlying cause.

  • Most deformities will correct with growth once the condition is treated.

  • Corrective surgery for severe deformities may be required.

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Publisher: Cambridge University Press
Print publication year: 2008

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