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...
| Main Authors: | , , , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Springer Netherlands
2010
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224720/ |