SAT0620 Further evidences of secondary amyloidosis in alkaptonuria
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DOI: 10.1136/annrheumdis-2018-eular.4645
Abstract: Background Alkaptonuria (AKU) is an ultra-rare inborn error of metabolism due to a deficient activity of homogentisate 1,2-dioxygenase. Patients suffer from a severe arthropathy. Evidence was provided on the presence of a secondary serum amyloid… read more here.
Keywords: amyloid; microscopy; analysis; aku patients ... See more keywords