Rationale: De Novo transplant amyloidosis denotes the condition when a patient develops amyloidosis after transplantation but had not been diagnosed with the disease prior to transplantation. The incidence of de novo amyloidosis in kidney transplants is rare, but few published case reports have described the occurrence of de novo Amyloid A protein (AA) and Light Chain (AL) amyloidosis. However, de novo hereditary fibrinogen A alpha chain (AFib) has not been previously reported. Patient Presentation: We present a 72-year-old man, a kidney transplant recipient, who developed progressive rise in his creatinine about 3 years after transplantation. He has long-standing diabetes mellitus type 2, obesity, and hypertension, so he did not have a kid...
International audienceAlthough end-stage renal disease related to AA amyloidosis nephropathy is well...
The fate of preexisting benign monoclonal gammopathy after organ transplantation is largely unknown....
A patient with familial Mediterranean fever and amyloidosis who received a cadaver renal transplant ...
Fibrinogen amyloidosis due to mutations in the fibrinogen -chain gene (AFib) localized on chromosome...
AA amyloidosis is a disorder characterized by the abnormal formation, accumulation and systemic depo...
Fibrinogen A alpha chain amyloidosis is an autosomal dominant disease associated with mutations in t...
Fibrinogen A alpha chain amyloidosis is an autosomal dominant disease associated with mutations in t...
Background: Fibrinogen A alpha-chain (AFib) amyloidosis is a rare and late-onset disease, that resu...
Background: Development of amyloidosis post solid-organ transplantation has not been reported, alt...
Copyright © 2015 Isabel Tavares et al. This is an open access article distributed under the Creative...
Systemic hereditary amyloidoses are autosomal dominant diseases associated with mutations in genes e...
International audienceHereditary systemic amyloidosis comprises several autosomal dominant diseases ...
The fate of preexisting benign monoclonal gammopathy after organ transplantation is largely unknown....
International audienceRationale & ObjectiveOutcomes of kidney transplantation for patients with rena...
Introduction: Amyloidosis is a disorder of protein folding in which normally soluble proteins underg...
International audienceAlthough end-stage renal disease related to AA amyloidosis nephropathy is well...
The fate of preexisting benign monoclonal gammopathy after organ transplantation is largely unknown....
A patient with familial Mediterranean fever and amyloidosis who received a cadaver renal transplant ...
Fibrinogen amyloidosis due to mutations in the fibrinogen -chain gene (AFib) localized on chromosome...
AA amyloidosis is a disorder characterized by the abnormal formation, accumulation and systemic depo...
Fibrinogen A alpha chain amyloidosis is an autosomal dominant disease associated with mutations in t...
Fibrinogen A alpha chain amyloidosis is an autosomal dominant disease associated with mutations in t...
Background: Fibrinogen A alpha-chain (AFib) amyloidosis is a rare and late-onset disease, that resu...
Background: Development of amyloidosis post solid-organ transplantation has not been reported, alt...
Copyright © 2015 Isabel Tavares et al. This is an open access article distributed under the Creative...
Systemic hereditary amyloidoses are autosomal dominant diseases associated with mutations in genes e...
International audienceHereditary systemic amyloidosis comprises several autosomal dominant diseases ...
The fate of preexisting benign monoclonal gammopathy after organ transplantation is largely unknown....
International audienceRationale & ObjectiveOutcomes of kidney transplantation for patients with rena...
Introduction: Amyloidosis is a disorder of protein folding in which normally soluble proteins underg...
International audienceAlthough end-stage renal disease related to AA amyloidosis nephropathy is well...
The fate of preexisting benign monoclonal gammopathy after organ transplantation is largely unknown....
A patient with familial Mediterranean fever and amyloidosis who received a cadaver renal transplant ...