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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Detalles Bibliográficos
Autores principales: Jamale, T. E., Hase, N. K., Kulkarni, M., Iqbal, A. M., Rurali, E., Kulkarni, M. G., Shetty, P., Pradeep, K. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495354/
https://www.ncbi.nlm.nih.gov/pubmed/23162276
http://dx.doi.org/10.4103/0971-4065.101257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495354/
https://www.ncbi.nlm.nih.gov/pubmed/23162276
http://dx.doi.org/10.4103/0971-4065.101257

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