 Nephritis, Hereditary
"Nephritis, Hereditary" 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 group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
| Descriptor ID |
D009394
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| MeSH Number(s) |
C12.706.742 C12.777.419.570.620 C13.351.875.742 C13.351.968.419.570.620 C16.131.939.742 C17.300.200.517
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| Concept/Terms |
Nephritis, Hereditary- Nephritis, Hereditary
- Hereditary Nephritides
- Hereditary Nephritis
- Nephritides, Hereditary
- Nephritis, Familial
- Familial Nephritides
- Familial Nephritis
- Nephritides, Familial
Alport Syndrome- Alport Syndrome
- Alport Syndromes
- Syndrome, Alport
- Syndromes, Alport
- Alport's Syndrome
- Alports Syndrome
- Syndrome, Alport's
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Below are MeSH descriptors whose meaning is more general than "Nephritis, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Nephritis, Hereditary".
This graph shows the total number of publications written about "Nephritis, Hereditary" by people in this website by year, and whether "Nephritis, Hereditary" 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 |
|---|
| 1990 | 0 | 1 | 1 | | 2003 | 0 | 1 | 1 | | 2005 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Nephritis, Hereditary" by people in Profiles.
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Chertow GM, Appel GB, Andreoli S, Bangalore S, Block GA, Chapman AB, Chin MP, Gibson KL, Goldsberry A, Iijima K, Inker LA, Knebelmann B, Mariani LH, Meyer CJ, Nozu K, O'Grady M, Silva AL, Stenvinkel P, Torra R, Warady BA, Pergola PE. Study Design and Baseline Characteristics of the CARDINAL Trial: A Phase 3 Study of Bardoxolone Methyl in Patients with Alport Syndrome. Am J Nephrol. 2021; 52(3):180-189.
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Chang A, Logar CM, Finn LS, Alpers CE, Seliger SL. A rare cause of necrotizing and crescentic glomerulonephritis in a young adult male. Am J Kidney Dis. 2005 May; 45(5):956-60.
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Rizk D, Chapman AB. Cystic and inherited kidney diseases. Am J Kidney Dis. 2003 Dec; 42(6):1305-17.
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Naparstek Y, Ben-Yehuda A, Madaio MP, Bar-Tana R, Schuger L, Pizov G, Neeman ZV, Cohen IR. Binding of anti-DNA antibodies and inhibition of glomerulonephritis in MRL-lpr/lpr mice by heparin. Arthritis Rheum. 1990 Oct; 33(10):1554-9.
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