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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מידע ביבליוגרפי
Main Authors: Jamale, T. E., Hase, N. K., Kulkarni, M., Iqbal, A. M., Rurali, E., Kulkarni, M. G., Shetty, P., Pradeep, K. J.
פורמט: Artigo
שפה:Inglês
יצא לאור: Medknow Publications & Media Pvt Ltd 2012
נושאים:
Case Report
גישה מקוונת: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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