Renal osteodystrophy is a bone pathology, characterized by defective mineralization, that results from kidney disease. Renal oseodystrophy comes in two different forms, high bone turnover and low bone turnover.
Signs and symptomsRenal osteodystrophy may exhibit no symptoms; if it does show symptoms, they include:
DiagnosisRenal osteodystrophy is usually diagnosed after treatment for end-stage renal disease begins. Blood tests will indicate decreased calcium and calcitriol and increased phosphate and parathyroid hormone. X-rays will also show bone features of renal osteodystropy (chondrocalcinosis at the knees and pubic symphysis, osteopenia and bone fractures) but may be difficult to differentiate from other conditions. PathogenesisRenal osteodystrophy results from low vitamin D levels, tertiary hyperparathyroidism or hyperphosphatemia, an abnormally elevated serum phosphate, combined with hypocalcaemia, low serum calcium, both of which are due to decreased excretion of phosphate by the damaged kidney. Differential diagnosisTo confirm diagnosis, renal osteodystrophy must be distinguished from:
TreatmentTreatment for renal osteodystrophy includes:
PrognosisRecovery from renal osteodystrophy has been observed post renal transplantation. Renal osteodystrophy is a chronic condition with a conventional hemodialysis schedule.[1] References
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