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Radiologic manifestations in alcaptonuria (1984)

Justesen, P. ; Andersen, P. E.

Springer

Skeletal radiology 11 (1984), S. 204-208

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ISSN: 1432-2161

Keywords: Alcaptonuria ; Ochronotic arthropathy

Source: Springer Online Journal Archives 1860-2000

Topics: Medicine

Notes: Abstract Alcaptonuria is a rare, hereditary disorder of amino acid metabolism, secondary to lack of homogentisic acid oxydase. As a consequence, there is ex accumulation of homogentisic acid, which is excreted in the urine and deposited in the connective tissues. This deposition results in ochronotic pigmentation and arthropathy, of which some characteristic radiological findings are demonstrated.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1007/BF00349495

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