2011
DOI: 10.1097/mnm.0b013e32834955df
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Nuclear medicine techniques in the assessment of alkaptonuria

Abstract: Alkaptonuria is a rare autosomal recessive disorder due to a lack of the enzyme homogentisate dioxygenase, leading to ochronosis, a process of accumulation of a melanin-like polymer of homogentisic acid in cartilage and other collagenous structures. Patients develop severe osteoarthropathy that resembles osteoarthritis. Although the diagnosis of alkaptonuria is not particularly challenging in view of the blue-black discolouration of visible connective tissue and the presence of homogentisic acid in urine, the … Show more

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Cited by 4 publications
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“…Recently, the importance of nuclear magnetic techniques in helping the diagnosis of ochronotic arthropathy [25] and the possible use of spine radiograph in the diagnosis and staging of ochronotic spondyloarthropathy [26] have been pointed out.…”
Section: Diagnosis Of Alkaptonuriamentioning
confidence: 99%
“…Recently, the importance of nuclear magnetic techniques in helping the diagnosis of ochronotic arthropathy [25] and the possible use of spine radiograph in the diagnosis and staging of ochronotic spondyloarthropathy [26] have been pointed out.…”
Section: Diagnosis Of Alkaptonuriamentioning
confidence: 99%