Atypical adult-onset methylmalonic acidemia and homocystinuria presenting as hemolytic uremic syndrome

Thrombotic microangiopathy (TMA) syndromes can be secondary to a multitude of different diseases. Most can be identified with a systematic approach and, when excluded, TMA is generally attributed to a dysregulation in the activity of the complement alternative pathways—atypical hemolytic uremic synd...

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Publicado en:CEN Case Rep
Autores principales: Navarro, David, Azevedo, Ana, Sequeira, Sílvia, Ferreira, Ana Carina, Carvalho, Fernanda, Fidalgo, Teresa, Vilarinho, Laura, Santos, Maria Céu, Calado, Joaquim, Nolasco, Fernando
Formato: Artigo
Lenguaje:Inglês
Publicado: Springer Japan 2018
Materias:
Case Report
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5886929/
https://ncbi.nlm.nih.gov/pubmed/29294253
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-017-0298-6
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