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Perioperative management of patient with alkaptonuria and associated multiple comorbidities
Alkaptonuria is a rare inherited genetic disorder of tyrosine metabolism characterized by a triad of homogentisic aciduria, ochronosis, and arthritis. The most common clinical manifestations of ochronosis involve the musculoskeletal, respiratory, airway, cardiovascular, genitourinary, cutaneous, and...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications Pvt Ltd
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3127314/ https://ncbi.nlm.nih.gov/pubmed/21772695 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0970-9185.81839 |
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