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A late and difficult diagnosis of ochronosis
Alkaptonuria is a rare autosomal recessive disorder of metabolism caused by deficiency of homogentisic acid oxidase and resulting in accumulation of homogentisic acid in collagenous structures. This causes the classic clinical triad: (1) homogentisic aciduria (urine blackens on standing when oxidize...
Autores principales: | Groseanu, L, Marinescu, R, Laptoiun, D, Botezatu, I, Staniceanu, F, Zurac, S, Ionescu, R |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Carol Davila University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3019075/ https://www.ncbi.nlm.nih.gov/pubmed/21254745 |
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