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Diagnosis of secondary amyloidosis in alkaptonuria
BACKGROUND: Alkaptonuria (AKU) is an inborn error of catabolism due to a deficient activity of homogentisate 1,2-dioxygenase. Patients suffer from a severe arthropathy, cardiovascular and kidney disease but other organs are affected, too. We found secondary amyloidosis as a life-threatening complica...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4189149/ https://ncbi.nlm.nih.gov/pubmed/25567001 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13000-014-0185-9 |
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