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Hereditary ADAMTS 13 deficiency presenting as recurrent acute kidney injury
We report here a case of 26-year-old male who presented with history of recurrent acute renal failure associated with microangiopathic hemolytic anemia and thrombocytopenia. ADAMTS 13 deficiency due to mutation in the gene encoding for ADAMTS 13 was identified as the cause. After eight episodes of a...
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| Main Authors: | , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Medknow Publications & Media Pvt Ltd
2012
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3495354/ https://ncbi.nlm.nih.gov/pubmed/23162276 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-4065.101257 |
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