 Nephrotic Syndrome
"Nephrotic Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction.
| Descriptor ID |
D009404
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| MeSH Number(s) |
C12.777.419.630.643 C13.351.968.419.630.643
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| Concept/Terms |
Nephrotic Syndrome- Nephrotic Syndrome
- Nephrotic Syndromes
- Syndrome, Nephrotic
- Syndromes, Nephrotic
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Below are MeSH descriptors whose meaning is more general than "Nephrotic Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Nephrotic Syndrome".
This graph shows the total number of publications written about "Nephrotic Syndrome" by people in this website by year, and whether "Nephrotic Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1981 | 0 | 1 | 1 | | 1984 | 1 | 1 | 2 | | 1985 | 0 | 1 | 1 | | 1987 | 0 | 1 | 1 | | 1989 | 2 | 0 | 2 | | 1991 | 0 | 1 | 1 | | 1997 | 2 | 0 | 2 | | 2001 | 0 | 1 | 1 | | 2003 | 1 | 0 | 1 | | 2004 | 1 | 0 | 1 | | 2005 | 3 | 2 | 5 | | 2011 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2018 | 2 | 0 | 2 | | 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Nephrotic Syndrome" by people in Profiles.
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Gerstle K, Hashmat S, Clardy C, Hageman JR. Pediatric Hypertension and End-Stage Renal Disease. Pediatr Ann. 2020 Jun 01; 49(6):e258-e261.
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Khalighi MA, Gallan AJ, Chang A, Meehan SM. Collapsing Glomerulopathy in Lambda Light Chain Amyloidosis: A Report of 2 Cases. Am J Kidney Dis. 2018 10; 72(4):612-616.
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Schöffel N, Liehr RM, Bünger C, Krüger K, Rubin D. [Nephrotic syndrome and microhematuria in a patient with nutcracker syndrome: Report of a case and review of the literature]. Internist (Berl). 2018 06; 59(6):608-614.
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Cabral DA, Canter DL, Muscal E, Nanda K, Wahezi DM, Spalding SJ, Twilt M, Benseler SM, Campillo S, Charuvanij S, Dancey P, Eberhard BA, Elder ME, Hersh A, Higgins GC, Huber AM, Khubchandani R, Kim S, Klein-Gitelman M, Kostik MM, Lawson EF, Lee T, Lubieniecka JM, McCurdy D, Moorthy LN, Morishita KA, Nielsen SM, O'Neil KM, Reiff A, Ristic G, Robinson AB, Sarmiento A, Shenoi S, Toth MB, Van Mater HA, Wagner-Weiner L, Weiss JE, White AJ, Yeung RS. Comparing Presenting Clinical Features in 48 Children With Microscopic Polyangiitis to 183 Children Who Have Granulomatosis With Polyangiitis (Wegener's): An ARChiVe Cohort Study. Arthritis Rheumatol. 2016 10; 68(10):2514-26.
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Dante S, Glunz C. An athletic adolescent girl with proteinuria and hypertension. Pediatr Ann. 2015 Mar; 44(3):e58-61.
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Westbroek EM, Mukerji N, Kalanithi P, Steinberg GK. Internal carotid artery surgical revascularization in a pediatric patient with Schimke immuno-osseous dysplasia. J Neurosurg Pediatr. 2015 Feb; 15(2):189-91.
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Okamoto K, Tokunaga K, Doi K, Fujita T, Suzuki H, Katoh T, Watanabe T, Nishida N, Mabuchi A, Takahashi A, Kubo M, Maeda S, Nakamura Y, Noiri E. Common variation in GPC5 is associated with acquired nephrotic syndrome. Nat Genet. 2011 May; 43(5):459-63.
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Furtado LV, Pysher T, Opitz J, Lamb R, Comstock J, Batish S, Mauch T, Nelson R, Zhou H. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene. Fetal Pediatr Pathol. 2011; 30(4):266-72.
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Horton AL, Smith JK, Strauss RA. Recurrence of Galloway Mowat syndrome and associated prenatal imaging findings. Prenat Diagn. 2009 Mar; 29(3):280-2.
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Gwin K, Cajaiba MM, Caminoa-Lizarralde A, Picazo ML, Nistal M, Reyes-Múgica M. Expanding the clinical spectrum of Frasier syndrome. Pediatr Dev Pathol. 2008 Mar-Apr; 11(2):122-7.
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