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Membranoproliferative glomerulonephritis and a rare bleeding disorder: factor X deficiency
Factor X (FX) deficiency is a rare hereditary coagulation disorder. This is the first case report on the association of FX deficiency and membranoproliferative glomerulonephritis (MPGN) type I. The patient, a 17-year-old male, presented with edema, hypertension, and microscopic hematuria, followed b...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Netherlands
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3224720/ https://ncbi.nlm.nih.gov/pubmed/20859684 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11255-010-9840-6 |
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