 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 UAMS Profiles 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 |
|---|
| 2024 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 | | 2014 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2005 | 0 | 1 | 1 |
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Below are the most recent publications written about "Nephritis, Hereditary" by people in Profiles over the past ten years.
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LeBleu VS, Kanasaki K, Lovisa S, Alge JL, Kim J, Chen Y, Teng Y, Gerami-Naini B, Sugimoto H, Kato N, Revuelta I, Grau N, Sleeman JP, Taduri G, Kizu A, Rafii S, Hochedlinger K, Quaggin SE, Kalluri R. Genetic reprogramming with stem cells regenerates glomerular epithelial podocytes in Alport syndrome. Life Sci Alliance. 2024 Jun; 7(6).
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Alge JL, Bekheirnia N, Willcockson AR, Qin X, Scherer SE, Braun MC, Bekheirnia MR. Variants in genes coding for collagen type IV a-chains are frequent causes of persistent, isolated hematuria during childhood. Pediatr Nephrol. 2023 03; 38(3):687-695.
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Gomez IG, MacKenna DA, Johnson BG, Kaimal V, Roach AM, Ren S, Nakagawa N, Xin C, Newitt R, Pandya S, Xia TH, Liu X, Borza DB, Grafals M, Shankland SJ, Himmelfarb J, Portilla D, Liu S, Chau BN, Duffield JS. Anti-microRNA-21 oligonucleotides prevent Alport nephropathy progression by stimulating metabolic pathways. J Clin Invest. 2015 Jan; 125(1):141-56.
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