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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Detalles Bibliográficos
Autores principales: Basturk, T., Ahbap, E., Eroglu Kesim, B., Yılmaz, M., Koç, Y., Sakacı, T., Unsal, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2010
Materias:
Nephrology – Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224720/
https://www.ncbi.nlm.nih.gov/pubmed/20859684
http://dx.doi.org/10.1007/s11255-010-9840-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224720/
https://www.ncbi.nlm.nih.gov/pubmed/20859684
http://dx.doi.org/10.1007/s11255-010-9840-6

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