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J Nephropathol. 2013;2(1): 73-74.
doi: 10.5812/nephropathol.8999
PMID: 24475429
PMCID: PMC3886177
Scopus ID: 84881082860
  Abstract View: 2557
  PDF Download: 1501

Commentary

Antiphospholipid Syndrome: A complex disease

Fátima Serrano*
*Corresponding Author: Email: fatima_serrano@hotmail.com

Implication for health policy/practice/research/medical education:

In the last three decades, a variety of clinical manifestations involving almost all organs and tissues (cardiac, pulmonary, neurological, renal, cutaneous, haematologic, gastrointestinal, ocular, skeletal and endocrinologic), have been described associated with antiphospholipid antibodies (aPL) . Nevertheless, the exact mechanism underlying the pathogenesis of aPL-mediated damage has been poorly recognized. Inflammatory mechanisms beyond thrombosis have been proposed in some clinical presentations, suggesting a role for immunomodulation in therapeutic strategy.

Please cite this paper as: Serrano F.Antiphospholipid Syndrome: A complex disease.J Nephropathology. 2013; 2(1): 73-74. DOI: 10.5812/nephropathol.8999

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ePublished: 01 Jan 2013
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