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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease focal segmental glomerulosclerosis
Comorbidity C0027726|nephrotic syndrome
Sentences 35
PubMedID- 23168861 An 18-year-old man presented with severe nephrotic syndrome due to focal segmental glomerulosclerosis.
PubMedID- 24856380 Results indicate possible clustering of causative nphs2 mutations in fsgs-proven srns with onset before age one year old, and provide additional evidence that patients with childhood steroid-resistant nephrotic syndrome due to focal segmental glomerulosclerosis should first undergo analysis of nphs2 coding sequence and wt1 exons 8 and 9 and surrounding exon/intron boundary sequences, followed by gender genotyping.
PubMedID- 24059478 We report a case of focal segmental glomerulosclerosis with nephrotic syndrome secondary to high-altitude polycythemia (hapc).
PubMedID- 24255611 Progressive declines in gfr are often associated with increasing proteinuria but the courseis different to that observed in nephrotic syndrome of idiopathic fsgs and minimal changedisease(2,9).
PubMedID- 20865462 nephrotic syndrome due to collapsing fsgs is a serious complication of treatment with bisphosphonates, especially of i.v.
PubMedID- 26005937 The first one is a disseminated strongyloidiasis occurred in an ecuadorian male on corticosteroid therapy for nephrotic syndrome due to focal segmental glomerulosclerosis, successfully treated with ivermectin; the second one involves another ecuadorian male affected by acute kidney failure and nephrotic syndrome in iga nephropathy with a diagnosis of chronic strongyloidiasis performed before starting the immunosuppressive treatment.
PubMedID- 22286071 Background/aims: minimal change disease (mcd) and focal segmental glomerulosclerosis (fsgs) are common causes of nephrotic syndrome (ns) in adults.
PubMedID- 20734088 In older patients cystinosis can mimic idiopathic nephrotic syndrome due to focal and segmental glomerulosclerosis.
PubMedID- 21904677 [90] reported an infantile steroid-resistant nephrotic syndrome associated with fsgs in three children with a homozygous haplotype in which two mutations are present in cis (p20l and r168h).
PubMedID- 26220221 Methods: a total of 120 fsgs patients with nephrotic syndrome were enrolled in this study.
PubMedID- 20567873 A 74-year-old man was diagnosed with nephrotic syndrome due to focal segmental glomerulosclerosis, and steroid therapy was initiated.
PubMedID- 23624956 Background: minimal change disease (mcd) and focal segmental glomerulosclerosis (fsgs) are common causes of nephrotic syndrome in children and adults.
PubMedID- 24381395 We present a patient with steroid-resistant nephrotic syndrome due to focal segmental glomerulosclerosis along with smoldering multiple myeloma.
PubMedID- 24009220 This report describes our experience using acth for nephrotic syndrome due to idiopathic fsgs in the united states.
PubMedID- 23901340 Subgroup 1 included 40 patients with steroid resistant nephrotic syndrome (histopathology of focal segmental glomerulosclerosis, fsgs) and subgroup 2 contained 39 kidney transplant recipients.
PubMedID- 20590696 At the age of three yr, a male patient had surgical treatment for bilateral vesicoureteral reflux (vur), and at the age of 19 yr, he developed nephrotic syndrome because of focal segmental glomerulosclerosis (fsgs).
PubMedID- 24666814 Of note, fsgs with nephrotic syndrome exhibits a grave prognosis; responsiveness to corticosteroids is not favorable compared to minimal change disease (mcd) and a substantial number of patients with fsgs develop esrd, especially in african americans [7].
PubMedID- 24771498 Tacrolimus therapy in adult-onset steroid-resistant nephrotic syndrome due to a focal segmental glomerulosclerosis single-center experience.
PubMedID- 25883898 His medical history revealed nephrotic syndrome due to focal segmental glomerulosclerosis, which was diagnosed 24 years previously and had progressed to chronic renal failure requiring dialysis therapy.
PubMedID- 22790456 Recent data suggests increased incidence of focal segmental glomerulosclerosis (fsgs) among children with idiopathic nephrotic syndrome (ins).
PubMedID- 26275234 Background: we investigated the efficacy of rituximab and low-dose cyclosporine combination therapy for focal segmental glomerulosclerosis (fsgs) children with steroid-resistant nephrotic syndrome (srns).
PubMedID- 24701046 We present a case of kin in a child, who was also found to have nephrotic syndrome because of focal segmental glomerulosclerosis on renal biopsy.
PubMedID- 23461215 [a case of focal segmental glomerulosclerosis with nephrotic syndrome after hematopoietic stem cell transplantatation for aplastic anemia].
PubMedID- 19921279 The diagnosis of frasier syndrome is based on the association of male pseudohermaphroditism (as a result of gonadal dysgenesis), with steroid-resistant nephrotic syndrome due to focal and segmental glomerular sclerosis (fsgs), which progresses to end-stage renal failure (esrf) during adolescence or adulthood.
PubMedID- 24719498 Nearly from seven to fifteen percent of all children affected by idiopathic nephrotic syndrome are diagnosed with fsgs after renal biopsy.
PubMedID- 22089787 A 12-year-old girl with a history of steroid and cyclosporine (csa) resistant nephrotic syndrome owing to focal and segmental glomerulosclerosis (fsgs) has progressed to end-stage renal disease (esrd) for which she underwent hemodialysis for 18 months before she successfully received a fully matched kidney transplant from her sister at the age of nine years.
PubMedID- 20590695 We diagnosed nephrotic syndrome due to recurrent fsgs with graft dysfunction and confirmed fsgs lesions with severe endothelial injury with an allograft biopsy, associated with calcineurin inhibitor (cni) nephrotoxicity.
PubMedID- 26167688 Plasma supar levels of igan and primary fsgs patients with nephrotic syndrome were not significantly different (p = 0.306).
PubMedID- 25880780 This is probably the first reported case to have chylous ascites, adult onset nephrotic syndrome with fsgs on renal histology and presence of lymphangiectasia in the same patient.
PubMedID- 24535024 In japan, ldl-a to control hyperlipidemia in patients with refractory nephrotic syndrome associated with focal segmental glomerulosclerosis is covered by national health insurance.
PubMedID- 20191367 We describe the novel association in a girl of nephrotic syndrome due to focal segmental glomerulosclerosis, bilateral sensorineural deafness, basal ganglia calcification, bilateral retinopathy similar to that seen in coats' disease, with de novo duplication of a subtelomeric region of chromosome 4q35.
PubMedID- 23602193 Motivated by a patient with subacute-onset nephrotic syndrome, histologic features of secondary focal segmental glomerulosclerosis, and concurrent mercury toxicity, we conducted a systematic review to explore renal histologic changes in patients with toxic mercury exposures and nephrotic syndrome.
PubMedID- 24093110 Urinary igg and alpha2-macroglobulin are powerful predictors of outcome and responsiveness to steroids and cyclophosphamide in idiopathic focal segmental glomerulosclerosis with nephrotic syndrome.
PubMedID- 24429405 Serum-soluble urokinase receptor levels do not distinguish focal segmental glomerulosclerosis from other causes of nephrotic syndrome in children.
PubMedID- 22693670 This autosomal recessive disorder is characterized by the autosomal recessive transmission of spondyloepiphyseal dysplasia and characteristic dysmorphic features, lymphocytopenia and/or t-cell immunodeficiency, and renal dysfunction including proteinuria and nephrotic syndrome due to fsgs [77].

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