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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease focal segmental glomerulosclerosis
Comorbidity C0022658|renal disease
Sentences 18
PubMedID- 26335292 Our results suggest that the aa genotype might be a risk factor for the progression of renal disease in fsgs and mcp1 genotyping may help the physicians to predict prognosis in these patients.
PubMedID- 20537521 Primary focal segmental glomerulosclerosis (fsgs) leads to end-stage renal disease in a high proportion of cases.
PubMedID- 25861251 Particularly in focal segmental glomerular sclerosis (fsgs), a frequent cause of end-stage renal disease with a prevalence of 4% in usa, podocytes are at significantly increased risk of injury and loss, a phenomenon called podocytopathy [5].
PubMedID- 24089165 Background: podocin mutations are characterized by progression to end stage renal disease and histologic findings of focal segmental glomerulosclerosis (fsgs).
PubMedID- 26069779 A 42-year-old male with end-stage renal disease due to focal segmental glomerulosclerosis received a single antigen-matched deceased kidney allograft transplant.
PubMedID- 21757990 He had history of end stage renal disease due to focal segmental glomerulosclerosis.
PubMedID- 22870165 A renal biopsy was done three months before admission which revealed interstitial renal disease with focal segmental glomerulosclerosis.
PubMedID- 25821763 A 26-year-old young female with end-stage renal disease due to focal segmental glomerulosclerosis on maintenance hemodialysis was admitted for malignant hypertension to our nephrology department.
PubMedID- 26337565 Expression of cell membrane antigens in cells excreted in the urinary sediment predicts progression of renal disease in patients with focal segmental glomerulosclerosis.
PubMedID- 24803921 We report the case of a 58-year-old male african-american patient who became dialysis dependent in 1990 after he had developed end-stage renal disease due to focal segmental glomerulosclerosis.
PubMedID- 24969201 Nphs2 mutations are associated with steroid-resistant nephrotic syndrome (srns), with the pathologic variant being focal and segmental glomerulosclerosis (fsgs), an emerging cause of end-stage renal disease in children.
PubMedID- 24701040 [4519] not only this, the proportion of fsgs as cause of end-stage renal disease in usa has increased almost ten times in the last two decades.
PubMedID- 21411799 Summary: a 23-year-old hispanic man who received a renal transplant from a living relative secondary to end-stage renal disease due to focal segmental glomerulosclerosis arrived at an outpatient clinic with gum swelling and pain.
PubMedID- 20835318 In this study only one patient with fsgs died because of end stage renal disease.
PubMedID- 25715638 Methods: we studied patients with end-stage renal disease (esrd) due to idiopathic fsgs, transplanted between 2001 and 2010.
PubMedID- 23984264 A 34-year-old man with end-stage renal disease as a result of the focal segmental glomerulosclerosis and uncontrolled hypertension that precluded the transplantation surgery and the patient's post-transplant blood pressure and the renal function remained within normal limits following the transplant for 6 months of follow-up.
PubMedID- 25964888 Moreover, a recent clinicopathological report on 127 patients from 11 large pedigrees found a definite association of heterozygous col4a3/col4a4 mutations with familial microscopic hematuria, chronic renal failure and end stage renal disease, due to fsgs, suggesting that the term “benign familial hematuria” is a misnomer, at least in their cohort (19,20).
PubMedID- 24069362 The frequency of end-stage renal disease in patients with fsgs was found to be as high as 78% in long-term follow-up studies [4,5].

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