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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 no: | CEN Case Rep |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Japan
2018
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| Assuntos: | |
| Acesso em linha: | 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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