• There are thought to be two forms of nephrotic syndrome, minimal change disease (MCD) and focal sclerosis (FSGS). (childrenshospital.org)
  • There are two main categories: minimal change disease (MCD) and focal sclerosis (FSGS). (childrenshospital.org)
  • In patients presenting with nephrotic syndrome , distinguishing focal segmental glomerulosclerosis (FSGS) from other glomerular diseases (eg, minimal-change disease, mesangial proliferative glomerulonephritis, membranoproliferative glomerulonephritis, membranous glomerulonephritis) is clinically difficult. (medscape.com)
  • In young Black men, FSGS is the commonest cause of nephrotic syndrome. (medscape.com)
  • In their study, levels of urinary NGAL, NAG, and RBP were higher in patients with FSGS (n=32) than in patients with minimal change nephrotic syndrome with comparable proteinuria (n=22). (medscape.com)
  • Some diseases that are "nephrotic" include idiopathic membranous nephropathy(IMN), minimal change nephropathy (MCN, most common in children), and focal and segmental glomerulosclerosis(FSGS,second most common in children). (greenmedinfo.com)
  • Data compiled during the 1970s and early 1980s indicated that during these periods, membranous nephropathy was the most common cause of unexplained nephrotic syndrome in adults, followed in order of frequency by minimal-change nephropathy and focal segmental glomerulosclerosis (FSGS). (scienceopen.com)
  • The entire EPPIK study (including FSGS, MCD, IgAN, IgAV and Alport Syndrome) will enroll approximately 57 children. (kidneyhealthgateway.com)
  • The goals of the study are to evaluate the safety and effectiveness of sparsentan on children with FSGS, MCD, IgAN, IgAV and Alport syndrome. (kidneyhealthgateway.com)
  • Focal segmental glomerulosclerosis (FSGS) is a frequent glomerular kidney disease that is revealed by proteinuria or even nephrotic syndrome. (nephcure.org)
  • This histopathological lesion may be caused by a primary podocyte injury (idiopathic FSGS) but is also associated with other pathologies (secondary FSGS). (nephcure.org)
  • The first-line treatment for idiopathic FSGS with nephrotic syndrome is a prolonged course of corticosteroids. (nephcure.org)
  • However, clinical experience and additional published data suggest that Acthar is effective at reducing proteinuria across multiple different idiopathic nephrotic syndrome etiologies including iMN, Focal Segmental Glomerular Sclerosis (FSGS), IgA Nephropathy, and Minimal Change Disease (MCD). (mallinckrodt.com)
  • We remain committed to making a difference in the lives of these very sick patients, as evidenced by the initiation of the largest FSGS clinical trial ever conducted, as well as fifteen Investigator Initiated research studies developing data on Acthar's utility across a broad spectrum of nephrotic syndrome etiologies, including recurrent post-transplant FSGS. (mallinckrodt.com)
  • Can you tell us what the evolution of FSGS is and how this has changed over the past decade or so? (medscape.com)
  • Primary FSGS classically presents with the nephrotic syndrome . (medscape.com)
  • In familial focal segmental glomerulosclerosis (FSGS), gain-of-function mutants of TRPC6 have been identified, and in steroid resistant nephrotic syndrome or idiopathic pulmonary arterial hypertension patients, a single nucleotide polymorphism in the promoter region that increases mRNA expression of TRPC6 has been identified (see for example: Pediatr Res. (justia.com)
  • Broadly, FSGS is divided into primary (idiopathic) and secondary forms. (biomedcentral.com)
  • In comparison with secondary FSGS, primary FSGS is more likely to present with nephrotic-range proteinuria and have a poorer prognosis, with 50% progressing to ESRD over 3-8 years ([ 9 , 10 ]. (biomedcentral.com)
  • For FSGS patients with nephrotic-range proteinuria, the use of corticosteroids is associated with an increased likelihood of a remission [ 9 , 11 ]. (biomedcentral.com)
  • Causes include a number of kidney diseases such as focal segmental glomerulosclerosis, membranous nephropathy, and minimal change disease. (wikipedia.org)
  • Nephrotic--range proteinuria may occur in other kidney diseases, such as IgA nephropathy. (medscape.com)
  • Although hematuria is the most common presentation in Whites with IgA nephropathy, nephrotic syndrome and renal insufficiency may also be present. (medscape.com)
  • Namely, because it admits the plausible association between circulating cationic bovine(cow) serum albumin (BSA, a common vaccine ingredient) and a very difficult-to-treat form of kidney disease called idiopathic membranous nephropathy (IMN). (greenmedinfo.com)
  • First, let me explain what nephrotic syndrome and membranous nephropathy are. (greenmedinfo.com)
  • The TANGO study will enroll adult (≥18 years) patients with a biopsy-proven primary Glomerular Disease (IgA nephropathy, Membranous glomerulonephritis, Focal and segmental glomerulosclerosis, Atypical hemolytic uremic syndrome, Membranoproliferative glomerulonephritis old classification type I-III, Complement- or IgG-positive membranoproliferative, glomerulonephritis, Dense-deposit disease, C3 glomerulonephritis) as the designated cause of their end-stage kidney disease who underwent a kidney transplant starting in January 2005 or later. (kidneyhealthgateway.com)
  • Histopathological diagnoses were focal segmental glomerulosclerosis (8), mesangial proliferative glomerulonephritis (4), IgM nephropathy (3), and minimal change disease (1). (nephcure.org)
  • Mallinckrodt has just completed such a process for a small Phase 4 pilot study that was begun by previous owners to generate potential new insights into the use of H.P. Acthar Gel in treatment of idiopathic Membranous Nephropathy (iMN), specifically in refractory patients who had failed previous immunosuppressive therapies. (mallinckrodt.com)
  • The dysregulated podocyte phenotype: a novel concept in the pathogenesis of collapsing idiopathic focal segmental glomerulosclerosis and HIV-associated nephropathy[J]. J Am Soc Nephrol, 1999, 10(1):51-61. (zjujournals.com)
  • Among all the types of glomerulonephritis, minimal-change nephropathy is most responsive to treatment. (basicmedicalkey.com)
  • The Membranous Nephropathy Trial of Rituximab (MENTOR) study is poised to change first-line-treatment recommendations for idiopathic membranous nephropathy. (renalandurologynews.com)
  • Membranous nephropathy remains the most common cause of adult-onset nephrotic syndrome. (renalandurologynews.com)
  • Idiopathic membranous nephropathy rarely affects children. (renalandurologynews.com)
  • Your study will focus on idiopathic membranous nephropathy. (renalandurologynews.com)
  • Because idiopathic membranous nephropathy means that no specific cause of the process can be determined, it is therefore considered to be a diagnosis of exclusion-i.e., you must rule out secondary causes. (renalandurologynews.com)
  • The natural history of the idiopathic form of MGN-membranous glomerulonephritis, which is another name for membranous nephropathy-is quite distinct. (renalandurologynews.com)
  • Background: Idiopathic membranous nephropathy remains the leading cause of nephrotic syndrome in Caucasian adults. (elsevierpure.com)
  • Rituximab, a monoclonal antibody that specifically targets CD20 on the surface of B-cells, is effective in achieving a complete remission of proteinuria in patients with idiopathic membranous nephropathy. (elsevierpure.com)
  • Discussion: This study will test for the first time whether treatment with rituximab is non-inferior to CSA in inducing long-term remission (complete or partial) of proteinuria in patients with idiopathic membranous nephropathy. (elsevierpure.com)
  • Genetic effect of the NPHS2 gene variants on proteinuria in minimal change disease and immunoglobulin A nephropathy. (cdc.gov)
  • Inhibition of TRPC6 activity may be particularly desirable in the treatment or prevention of a variety of diseases including nephrotic syndrome, focal segmental glomerulosclerosis, membranous nephropathy, diabetic nephropathy, heart failure, stroke, acute lung injury, acute respiratory distress syndrome (ARDS) and acute renal failure. (justia.com)
  • We present a case with a rare variant of glomerulonephritis, IgM nephropathy, which occurs mainly with nephrotic syndrome. (ter-arkhiv.ru)
  • Nephrotic syndrome has many causes, including primary kidney diseases such as minimal-change disease , focal segmental glomerulosclerosis , and membranous glomerulonephritis . (medscape.com)
  • APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries. (medscape.com)
  • Notably, the latest research shows that complement is also activated in kidney diseases that are not traditionally thought of as immune-mediated, including haemolytic-uraemic syndrome, diabetic kidney disease and focal segmental glomerulosclerosis. (bvsalud.org)
  • We now know that among African Americans with nephrotic syndrome, certain variants of the gene APOL1 increase the likelihood of developing focal segmental glomerulosclerosis and progressing to end-stage renal disease. (cdc.gov)
  • Reduced podocin expression in minimal change disease and focal segmental glomerulosclerosis is related to the level of proteinuria[J]. Clin Exp Nephrol, 2013, 17(6):811-818. (zjujournals.com)
  • TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease. (cdc.gov)
  • 3. Srivastava T., Simon S.D., Alon U.S. High incidence of focal segmental glomerulosclerosis in neph rotic syndrome of childhood. (nephrolog.ru)
  • 4. Moura L.R.R., Franco M.F., Kirsztajn G.M. Minimal change disease and focal segmental glomerulosclerosis in adults: response to steroids and risk of renal failure. (nephrolog.ru)
  • 9. Siegel N.J., Kashgarian M., Spargo B.H. Minimal change and focal sclerotic lesions in lipoid nephrosis. (nephrolog.ru)
  • Glomerular tip lesion: a distinct entity within the minimal change disease/focal segmental glomerulosclerosis spectrum. (nephrolog.ru)
  • While most forms of nephrotic syndrome are idiopathic, meaning that the cause is unknown, some are inherited, meaning that they have a genetic cause. (cdc.gov)
  • Nephrotic syndrome may affect adults and children of both sexes and of any race. (medscape.com)
  • Patients who respond (ie, have cessation of proteinuria or a diuresis if edema is present) should continue prednisone for another 2 weeks and change to a maintenance regimen to minimize toxicity (2 to 3 mg/kg on alternate days for 4 to 6 weeks in children and for 8 to 12 weeks in adults, tapering during the next 4 months). (msdmanuals.com)
  • The classic teaching is that this is a histologic pattern of injury and not a disease per se, and nephrology is certainly going through a lot of revolutionary changes in this regard. (medscape.com)
  • Nephrotic syndrome can be primary, being a disease specific to the kidneys, or it can be secondary, being a renal manifestation of a systemic general illness. (medscape.com)
  • Nephrotic Syndrome can be "primary" or "secondary" in nature. (kidneyhealthgateway.com)
  • MPGN may be idiopathic or secondary in etiology. (medscape.com)
  • [ 1 ] The secondary types are more common than the idiopathic types and are diagnosed by carefully reviewing clinical features, laboratory data, and renal histopathology. (medscape.com)
  • Nephrotic syndrome may be due to a disease that causes primary glomerular injury (primary) or glomerular injury as part of a wider systemic process (secondary). (pulsenotes.com)
  • Confusingly, some causes of primary nephrotic syndrome may also occur as a secondary adaptive response to a systemic illness. (pulsenotes.com)
  • A clinical and histopathological study was performed on ninety-four patients with nephrotic syndrome (91 idiopathic and 3 secondary) who were admitted to Department of Internal Medicine, Yeungnam University Hospital during the period of nine years, from January 1985 to May 1994. (e-jyms.org)
  • The development of severe nephrotic syndrome at the beginning of the disease, the formation of secondary steroid resistance have confirmed this hypothesis and have justified the treatment with cyclosporin A aimed at the recovery of the function of the podocyte with remission of nephritis. (ter-arkhiv.ru)
  • It differs from nephritic syndrome in that there are no red blood cells in the urine. (wikipedia.org)
  • Actual urinary complaints such as haematuria or oliguria are uncommon, though these are seen commonly in nephritic syndrome. (wikipedia.org)
  • It may occur in typical form, or in association with nephritic syndrome. (medscape.com)
  • Nephrin redistribution on podocytes is a potential mechanism for proteinuria in patients with primary acquired nephritic syndrome[J]. Am J Pathol, 2001, 158(5):1723-1731. (zjujournals.com)
  • The signs and symptoms associated with glomerulonephritis can be nephritic in nature, characterized by inflammatory injury, or nephrotic in nature, characterized by proteinuria. (basicmedicalkey.com)
  • From a therapeutic perspective, nephrotic syndrome may be classified as steroid sensitive, steroid resistant, steroid dependent, or frequently relapsing. (medscape.com)
  • We conducted a prospective study on idiopathic nephrotic syndrome (INS) to explore the changes in the urine IL levels of the patients to discover the noninvasive indicators for predicting and dynamically monitoring steroid efficacy in the steroid therapy of INS patients. (uwi.edu)
  • The study aimed to explore the correlation between urine interleukin (IL)-8, 6, 10, 17 levels and the efficacy of steroid in patients with idiopathic nephrotic syndrome (INS). (uwi.edu)
  • Steroid-resistant nephrotic syndrome (SRNS) is an important cause of chronic kidney disease (CKD) in children that often progresses to end-stage renal disease (ESRD). (nephcure.org)
  • The response to steroid therapy was most effective in the patients with minimal change lesion. (e-jyms.org)
  • In response to glucocorticoid therapy, clinically idiopathic NS is defined as steroid-sensitive or steroid-resistant. (biochemia-medica.com)
  • The majority of paediatric idiopathic NS is steroid-sensitive which means that the symptoms of proteinuria, hypoalbuminemia and oedema will decrease within a few weeks of therapy (remission). (biochemia-medica.com)
  • Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome. (cdc.gov)
  • Steroid-resistant nephrotic syndrome: impact of genetic testing. (cdc.gov)
  • Here, we report on biallelic mutations in nine affected individuals who are from five unrelated families and show early-onset steroid-resistant nephrotic syndrome (SRNS). (edrc2013.org)
  • Steroid-dependent nephrotic syndrome in children: histopathology and relapses after cyclophosphamide treatment. (nephrolog.ru)
  • The research project has shown that just one dose of gene therapy targeting cells in the kidney has the potential to cure a condition known as steroid-resistant nephrotic syndrome. (nstrust.co.uk)
  • This work offers real hope for patients impacted by steroid-resistant nephrotic syndrome and potentially other genetic kidney diseases too. (nstrust.co.uk)
  • Studies of familial cases have identified both autosomal dominant and recessive forms and have led to the discovery of at least seven genes associated with inherited nephrotic syndrome. (cdc.gov)
  • Genomics could address health equity by replicating such community engagement strategies for topics such as family health history or specific hereditary conditions, for example, hereditary breast and ovarian cancer , Lynch syndrome , or familial hypercholesterolemia . (cdc.gov)
  • Nephrotic syndrome can also result from systemic diseases that affect other organs in addition to the kidneys, such as diabetes, amyloidosis, and lupus erythematosus. (medscape.com)
  • Nephrotic syndrome always affects both kidneys. (childrenshospital.org)
  • Nephrotic syndrome is a condition where the kidneys leak large amounts of protein into the urine and is defined in detail HERE . (greenmedinfo.com)
  • Zebrafish with knockdown generated by morpholino oligonucleotides displayed hypoplastic glomerulus structures Oxoadipic acid and abnormal podocyte foot processes, thereby mimicking the pathological changes seen in the kidneys of the SRNS individuals with mutations. (edrc2013.org)
  • Lipiduria (lipids in urine) can also occur, but is not essential for the diagnosis of nephrotic syndrome. (wikipedia.org)
  • The diagnosis of nephrotic syndrome is based on the identification of the typical triad . (pulsenotes.com)
  • Greater awareness of this cross-system syndrome should facilitate earlier diagnosis and more timely use of effective treatment. (lu.se)
  • r\nIrritable bowel syndrome (IBS) is a diagnosis of exclusion after other conditions have been ruled out. (dummies.com)
  • It is an idiopathic condition in paediatric patients characterized by proteinuria, hypoalbuminemia, oedema and hyperlipidaemia ( 1 ). (biochemia-medica.com)
  • Introduction Nephrotic syndrome (NS) is usually a renal disease caused by disruption of the glomerular filtration barrier, which results in massive proteinuria, hypoalbuminemia, and dyslipidemia. (edrc2013.org)
  • Nephrotic-range proteinuria is the loss of 3 grams or more per day of protein into the urine or, on a single spot urine collection, the presence of 2 g of protein per gram of urine creatinine. (medscape.com)
  • While nephrotic syndrome is not a disease , it can be the first sign of disease that can damage the kidney's tiny blood-filtering unit (glomeruli) where urine is made. (childrenshospital.org)
  • Nephrotic Syndrome can typically be diagnosed with a urine test. (kidneyhealthgateway.com)
  • Albumin is lost in the urine of patients with minimal change disease more so than larger serum proteins, probably because the disease causes changes in the charge barrier that affect albumin selectively. (msdmanuals.com)
  • Children with nephrotic syndrome have kidney damage that causes them to pass too much of a protein called albumin in their urine. (cdc.gov)
  • Nephrotic syndrome is a condition where the kidney's filtering units are damaged, allowing large amounts of protein that should be kept in the bloodstream to leak into the urine. (nstrust.co.uk)
  • Correlation between Chinese medicine syndromes and the NPHS1 gene and NPHS2 gene polymorphism as well as corticosteroid sensitivity in patients with minimal change disease]. (cdc.gov)
  • Identification of patients with minimal change nephrotic syndromefrom initial response to prednisone. (nephrolog.ru)
  • Thrombotic microangiopathy with hypertension and acute renal failure in children (a typical hemolytic uremic syndrome). (jpgmonline.com)
  • Guillain-Barré syndrome (GBS) can be described as a collection of clinical syndromes that manifests as an acute inflammatory polyradiculoneuropathy with resultant weakness and diminished reflexes. (medscape.com)
  • Taken together, the data suggest that this syndrome is a clinical expression of a self-limited primary immune-deficiency disease. (scienceopen.com)
  • The purpose of this website is to help patients with rare forms of primary Nephrotic Syndrome get connected to expert care and cutting-edge treatment options. (kidneyhealthgateway.com)
  • Change the primary and within fair. (myjuicecup.com)
  • Impact of the 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene on primary nephrotic syndrome. (cdc.gov)
  • 1. The primary nephrotic syndrome in children. (nephrolog.ru)
  • This, essentially intimal changes, is seen in diverse conditions and appears to result from primary endothelial injury followed by intimal exudation, thrombosis, and repair by fibrosis. (jpgmonline.com)
  • Kidney diseases that affect tubules and interstitium, such as interstitial nephritis, will not cause nephrotic syndrome. (medscape.com)
  • Nephrotic syndrome is neither a single gested that IL-1 has a significant role in the disease nor even a heterogeneous group of immunopathogenesis of proteinuria [ 7 ] and related diseases. (who.int)
  • Doctors often call these diseases "idiopathic," which means that they arise from an unknown cause. (kidneyhealthgateway.com)
  • Genomics provides opportunities to prevent, treat, or manage diseases by identifying genetic changes before signs or symptoms of disease occur. (cdc.gov)
  • The CTLA-4 +49GG genotype is associated with susceptibility for nephrotic kidney diseases. (cdc.gov)
  • The lack of evidence of a humoral antibody response, remission induced by measles which modifies cell-mediated immunity, the therapeutic benefits of steroids and cyclophosphamide which also abate cell-mediated responses, and the occurrence of this syndrome in Hodgkin's disease support this hypothesis. (scienceopen.com)
  • Inducing a diuresis or a remission of proteinuria in nephrotic syndrome without uremia of the idiopathic type or that due to lupus erythematosus. (mallinckrodt.com)
  • The aim of this study was to investigate lipoprotein particle distributions and the likelihood of achieving cholesterol homeostasis in the remission phase of nephrotic syndrome (NS) in paediatric patients. (biochemia-medica.com)
  • Favourable changes in the serum lipid profiles, HDL particle subclass distribution and cholesterol metabolism in paediatric patients with NS during remission took place. (biochemia-medica.com)
  • For the first time, we found that cholesterol homeostasis changed in favour of increased cholesterol absorption during disease remission. (biochemia-medica.com)
  • The efficacy of treatment will be assessed by the remission status (based on changes in proteinuria) at 24 months from randomization. (elsevierpure.com)
  • Atypical hemolytic-uremic syndrome (aHUS) is a chronic systemic disease of a genetic nature, which is based on uncontrolled activation of the alternative complement pathway, leading to generalized thrombosis in the vessels of the microvasculature (complement-mediated thrombotic microangiopathy). (ter-arkhiv.ru)
  • In addition, hyperlipidaemia, increased risk of venous/arterial thrombosis and higher risk of infection is typical of the syndrome. (pulsenotes.com)
  • white lines (leukonychia) that extend all the way across the nail and lie parallel to the lunula The main signs of nephrotic syndrome are: A proteinuria of greater than 3.5 g /24 h /1.73 m2 (between 3 and 3.5 g/24 h /1.73 m2 is considered to be proteinuria in the nephrotic range) or greater than 40 mg/h/m2 in children. (wikipedia.org)
  • ABSTRACT We studied 60 children affected with idiopathic nephrotic syndrome (INS) plus 20 age and sex matched controls. (who.int)
  • 10%. In the remaining 10% of children with lecular weight protein found on the surface nephrotic syndrome, it is largely mediated of all nucleated cells which synthesize it. (who.int)
  • minimal change nephrotic reabsorption and increased urinary excre- syndrome is most common in children 2-4 tion of -2-m [ 11 ]. (who.int)
  • In the vast majority of children, NS is idiopathic, meaning that doctors don't yet know what causes it. (childrenshospital.org)
  • Idiopathic nephrotic syndrome-the kind most children have-occurs for a reason that is unknown. (childrenshospital.org)
  • Studies in the U.S. have found higher rates of nephrotic syndrome in children of African descent, compared with children of European descent. (cdc.gov)
  • Nephrotic syndrome (NS) is a glomerular disorder affecting between 2-7 per 100,000 children below 16 years of age worldwide ( 1 ). (biochemia-medica.com)
  • Interleukin-13 genetic polymorphisms in Singapore Chinese children correlate with long-term outcome of minimal-change disease. (cdc.gov)
  • Angiotensin-converting enzyme genotype is not a significant genetic risk factor for idiopathic nephrotic syndrome in Croatian children. (cdc.gov)
  • Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children. (cdc.gov)
  • Often the symptoms can be managed with a type of medication known as steroids, however, around 10% of children with nephrotic syndrome do not respond to steroids and many will go on to develop kidney failure and will need dialysis or transplant within 2-5 years. (nstrust.co.uk)
  • The discovery could bring major benefits to many children who currently suffer from nephrotic syndrome. (nstrust.co.uk)
  • Thus I would like to conclude by saying that an idiopathic form of obliterative renal arteriopathy account for the rare presentation of severe hypertension and progressive renal failure with or without overt hemolytic anemia and thrombocytopenia in children. (jpgmonline.com)
  • Kappa B gene sequences can be activated by external microbes, antigens through acting potocytes, which can induce the upregulation of CD80 expression, cytoskeletal protein damage and the glomerular filtration rate changes, resulting in proteinuria. (zjujournals.com)
  • Here you see conditions such as irritable bowel syndrome (IBS), ischemic bowel, inflammatory bowel disease (IBD), celiac disease, and diverticulitis. (dummies.com)
  • Changing etiologies of unexplained adult nephrotic syndrome: a comparison of renal biopsy findings from 1976-1979 and 1995-1997. (scienceopen.com)
  • Minimal change disease (MCD) is a common pathological type of nephrotic syndrome. (zjujournals.com)
  • Diabetes is still the most common cause for a patient having nephrotic syndrome and nephrotic range proteinuria . (medscape.com)
  • We show that CNTN1, found in peripheral nerves and kidney glomeruli, is a common target for autoantibody-mediated pathology and may account for between 1 and 2% of idiopathic MGN cases. (lu.se)
  • This paper has been published under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International ( CC BY-NC-ND 4.0 ) allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially. (amjcaserep.com)
  • A very common syndrome associated with IBS is fibromyalgia syndrome. (dummies.com)
  • In an observational study we investigated the pathobiology and extent of this potential cause of MGN by examining the association of antibodies against CNTN1 with the clinical features of a cohort of 468 patients with suspected immune-mediated neuropathies, 295 with idiopathic MGN, and 256 controls. (lu.se)
  • minimal change nephrotic syndrome possible at present to distinguish whether is found in approximately 85% of INS, IL-6 contributes to renal dysfunction or mesangial proliferative glomerulonephritis whether it reflects renal damage [ 10 ]. (who.int)
  • positive serum tests for infectious mononucleosis (im) unaccompanied by the clinical syndrome or blood changes characteristic of the disease were detected in 39/177 (22%) mentally subnormal patients investigated with three different commercially available im slide tests. (liverpool.ac.uk)
  • Nephrotic syndrome results in increased concentrations of total serum cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), triglycerides (TG) and a variable concentration of serum high-density lipoprotein cholesterol (HDL-C) ( 2 ). (biochemia-medica.com)
  • Altered ultrastructural distribution of nephrin in minimal change nephrotic syndrome[J]. Nephrol Dial Transplant, 2003, 18(1):70-76. (zjujournals.com)