Alkaptonuria (Ochronosis)

Josephina A. Vossen

in Musculoskeletal Imaging Volume 1

Published on behalf of Oxford University Press

Published in print April 2019 | ISBN: 9780190938161
Published online June 2019 | e-ISBN: 9780190095772 | DOI:

Series: Rotations in Radiology

Alkaptonuria (Ochronosis)

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Chapter 39 discusses alkaptonuria (ochronosis), a rare hereditary metabolic disease that leads to the deposition of homogentisic acid. Homogentisic acid accumulation causes damage to connective tissues; leads to formation of renal, urethral, and prostatic calculi; causes cardiovascular abnormalities; and causes arthropathy. Ochronotic arthropathy is the articular manifestation of alkaptonuria with the most common clinical sites of involvement being the spine, knees, and hips. Diagnosis of the disease is made by demonstration of homogentisic acid in the urine. Radiography is the standard method for detecting changes associated with alkaptonuria. CT can aid in the detection of intervertebral disc calcification.

Chapter.  572 words.  Illustrated.

Subjects: Radiography

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