# Editorial: Case reports in nephrology

**Authors:** Sree Bhushan Raju, Manish Rathi, Sandeep Mahajan

PMC · DOI: 10.3389/fmed.2023.1278138 · Frontiers in Medicine · 2024-01-29

## Full-text entities

- **Genes:** PLA2R1 (phospholipase A2 receptor 1) [NCBI Gene 22925] {aka CLEC13C, PLA2-R, PLA2G1R, PLA2IR, PLA2R}, IL6R (interleukin 6 receptor) [NCBI Gene 3570] {aka CD126, HIES5, IL-1Ra, IL-6R, IL-6R-1, IL-6RA}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, UMOD (uromodulin) [NCBI Gene 7369] {aka ADMCKD2, ADTKD1, FJHN, HNFJ, HNFJ1, MCKD2}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** GI adverse (MESH:D005767), glomerulonephritis (MESH:D005921), anemia (MESH:D000740), intrauterine growth retardation (MESH:D005317), cystine stones (MESH:D003554), RAVT (MESH:D012170), UTI (MESH:D014552), colon rupture (MESH:D012421), renal colic (MESH:D056844), AKI (MESH:D058186), systemic and polyclonal lymphoproliferative disease (MESH:D008232), venous thrombosis (MESH:D020246), hyperphosphatemia (MESH:D054559), rheumatic autoimmune disorder (MESH:D012216), CKD (MESH:D051436), Nephrotic syndrome (MESH:D009404), multiorgan failure (MESH:D051437), immunoglobulin light-chain amyloidosis nephropathy (MESH:D000075363), calculous renal disease (MESH:D007674), Genetic diseases (MESH:D030342), GI bleeding (MESH:D006471), PTC (MESH:D000077273), death (MESH:D003643), bone marrow suppression (MESH:D001855), bacterial infection (MESH:D001424), autoimmune hemolytic anemia (MESH:D000744), hypocalcemia (MESH:D006996), MCD (MESH:D009402), malignancies (MESH:D009369), Infection (MESH:D007239), immune-complex glomerulonephritis (MESH:D007105), Pregnancy and renal diseases (MESH:D011254), renal emergencies (MESH:D004630), secondary hyperparathyroidism (MESH:D006962), skin disorders (MESH:D012871), EPN (MESH:D011704), septic shock (MESH:D012772), COVID (MESH:D000086382), amyloid nephropathy (MESH:C000718787), beta-thalassemia (MESH:D017086), Idiopathic multicentric Castleman disease (MESH:C537372), Cystinuria (MESH:D003555), INS (MESH:C535761), AON (MESH:D000208), sepsis (MESH:D018805), ESKD (MESH:D007676), membranous glomerulonephritis (MESH:D015433)
- **Chemicals:** Congo red (MESH:D003224), Rituximab (MESH:D000069283), calcium (MESH:D002118), cystine (MESH:D003553), tocilizumab (MESH:C502936), Chinese herbal medicine (-), creatinine (MESH:D003404), steroid (MESH:D013256), phosphate (MESH:D010710), Sevelamer carbonate (MESH:D000069603), apixaban (MESH:C522181), oxalate (MESH:D010070), prednisolone (MESH:D011239), cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606], Tripterygium wilfordii (species) [taxon 458696]
- **Mutations:** c.280T>C

## Full text

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## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC10859465/full.md

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Source: https://tomesphere.com/paper/PMC10859465