{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T13:08:26Z","timestamp":1762866506779,"version":"build-2065373602"},"reference-count":42,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,11,11]]},"DOI":"10.7759\/cureus.96561","type":"journal-article","created":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T12:55:21Z","timestamp":1762865721000},"source":"Crossref","is-referenced-by-count":0,"title":["Renaming Medullary Cystic Kidney Disease: A Review of Semantic Nomenclature"],"prefix":"10.7759","author":[{"given":"Kevin","family":"Kuang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sonika","family":"Vatsa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rahul","family":"Ramakrishnan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ahmik","family":"Shenoy","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohammadali M","family":"Shoja","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ghaith","family":"Al-Eyd","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","article-title":"Medullary cystic disease","volume":"5","author":"Devarajan P","year":"2020","unstructured":"Devarajan P. Medullary cystic disease. Medscape. 2020, 5:9.","journal-title":"Medscape"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1097\/RUQ.0000000000000366","article-title":"Ultrasound, computed tomography, and magnetic resonance imaging in a patient with medullary cystic kidney disease","volume":"34","author":"Whang G","year":"2018","unstructured":"Whang G, Tchelepi H. Ultrasound, computed tomography, and magnetic resonance imaging in a patient with medullary cystic kidney disease. Ultrasound Q. 2018, 34:288-91. 10.1097\/RUQ.0000000000000366","journal-title":"Ultrasound Q"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1001\/archpedi.1945.02020180033006","article-title":"Congenital medullary cysts of the kidneys with severe refractory anemia","volume":"69","author":"Smith CH","year":"1945","unstructured":"Smith CH, Graham JB. Congenital medullary cysts of the kidneys with severe refractory anemia. Am J Dis Child. 1945, 69:369-77. 10.1001\/archpedi.1945.02020180033006","journal-title":"Am J Dis Child"},{"key":"ref4","article-title":"Familial, juvenile nephronophthisis (idiopathic parenchymal contracted kidney)","volume":"6","author":"Fanconi G","year":"1951","unstructured":"Fanconi G, Hanhart E, von Albertini A, Uhlinger E, Dolivo G, Prader A. Familial, juvenile nephronophthisis (idiopathic parenchymal contracted kidney). Helv Paediatr Acta. 1951, 6:1-49.","journal-title":"Helv Paediatr Acta"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM196710192771606","article-title":"Medullary cystic disease and familial juvenile nephronophthisis","volume":"277","author":"Strauss MB","year":"1967","unstructured":"Strauss MB, Sommers SC. Medullary cystic disease and familial juvenile nephronophthisis. N Engl J Med. 1967, 277:863-4. 10.1056\/NEJM196710192771606","journal-title":"N Engl J Med"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.1962.tb06582.x","article-title":"Familial juvenile nephronophthisis","volume":"51","author":"Sydow GV","year":"1962","unstructured":"Sydow GV, Ranstrom S. Familial juvenile nephronophthisis. Acta Paediatr (Stockh). 1962, 51:561-74. 10.1111\/j.1651-2227.1962.tb06582.x","journal-title":"Acta Paediatr (Stockh)"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1001\/archinte.1952.00240120025003","article-title":"Studies of sodium and potassium metabolism in salt-losing nephritis","volume":"90","author":"Murphy RV","year":"1952","unstructured":"Murphy RV, Coffman EW, Pringle BH, Iseri LT. Studies of sodium and potassium metabolism in salt-losing nephritis. AMA Arch Intern Med. 1952, 90:750-62. 10.1001\/archinte.1952.00240120025003","journal-title":"AMA Arch Intern Med"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.7326\/0003-4819-57-3-373","article-title":"Clinical and pathological aspects of cystic disease of the renal medulla. An analysis of eighteen cases","volume":"57","author":"Strauss MB","year":"1962","unstructured":"Strauss MB. Clinical and pathological aspects of cystic disease of the renal medulla. An analysis of eighteen cases. Ann Intern Med. 1962, 57:373-81. 10.7326\/0003-4819-57-3-373","journal-title":"Ann Intern Med"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM196605052741802","article-title":"Hereditary occurrence of cystic disease of the renal medulla","volume":"274","author":"Goldman SH","year":"1966","unstructured":"Goldman SH, Walker SR, Merigan TC Jr, Gardner KD Jr, Bull JM. Hereditary occurrence of cystic disease of the renal medulla. N Engl J Med. 1966, 274:984-92. 10.1056\/NEJM196605052741802","journal-title":"N Engl J Med"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM196605052741813","article-title":"Cystic diseases of the kidney","volume":"274","year":"1966","unstructured":"Cystic diseases of the kidney. N Engl J Med. 1966, 274.1029-30. 10.1056\/NEJM196605052741813","journal-title":"N Engl J Med"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1136\/pgmj.44.516.792","article-title":"Medullary cystic disease of the kidney: its occurrence in two siblings","volume":"44","author":"Handa SP","year":"1968","unstructured":"Handa SP, Tennant R. Medullary cystic disease of the kidney: its occurrence in two siblings. Postgrad Med J. 1968, 44:792-8. 10.1136\/pgmj.44.516.792","journal-title":"Postgrad Med J"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1007\/s004670000518","article-title":"New insights: nephronophthisis-medullary cystic kidney disease","volume":"16","author":"Hildebrandt F","year":"2001","unstructured":"Hildebrandt F, Omram H. New insights: nephronophthisis-medullary cystic kidney disease. Pediatr Nephrol. 2001, 16:168-76. 10.1007\/s004670000518","journal-title":"Pediatr Nephrol"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1001\/jama.1975.03250060025016","article-title":"Medullary cystic disease vs nephronophthisis. A valid distinction?","volume":"232","author":"Giangiacomo J","year":"1975","unstructured":"Giangiacomo J, Monteleone PL, Witzleben CL. Medullary cystic disease vs nephronophthisis. A valid distinction?. JAMA. 1975, 232:629-31. 10.1001\/jama.1975.03250060025016","journal-title":"JAMA"},{"key":"ref14","article-title":"Juvenile nephronophthisis and medullary cystic disease","volume":"52","author":"Chamberlin BC","year":"1977","unstructured":"Chamberlin BC, Hagge WW, Stickler GB. Juvenile nephronophthisis and medullary cystic disease. Mayo Clin Proc. 1977, 52:485-91.","journal-title":"Mayo Clin Proc"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.1093\/ndt\/12.6.1242","article-title":"Late occurrence of cysts in autosomal dominant medullary cystic kidney disease","volume":"12","author":"Neumann HP","year":"1997","unstructured":"Neumann HP, Z\u00e4uner I, Strahm B, et al.. Late occurrence of cysts in autosomal dominant medullary cystic kidney disease. Nephrol Dial Transplant. 1997, 12:1242-6. 10.1093\/ndt\/12.6.1242","journal-title":"Nephrol Dial Transplant"},{"key":"ref16","doi-asserted-by":"publisher","DOI":"10.1007\/s00467-008-0840-z","article-title":"Nephronophthisis","volume":"24","author":"Salomon R","year":"2009","unstructured":"Salomon R, Saunier S, Niaudet P. Nephronophthisis. Pediatr Nephrol. 2009, 24:2333-44. 10.1007\/s00467-008-0840-z","journal-title":"Pediatr Nephrol"},{"key":"ref17","doi-asserted-by":"publisher","DOI":"10.1016\/s0022-5347(17)43510-5","article-title":"Renal dysgenesis and cystic disease of the kidney: a report of the Committee on Terminology, Nomenclature and Classification, Section on Urology, American Academy of Pediatrics","volume":"138","author":"Glassberg KI","year":"1987","unstructured":"Glassberg KI, Stephens FD, Lebowitz RL, et al.. Renal dysgenesis and cystic disease of the kidney: a report of the Committee on Terminology, Nomenclature and Classification, Section on Urology, American Academy of Pediatrics. J Urol. 1987, 138:1085-92. 10.1016\/s0022-5347(17)43510-5","journal-title":"J Urol"},{"key":"ref18","doi-asserted-by":"publisher","DOI":"10.1038\/ng0493-342","article-title":"A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p","volume":"3","author":"Antignac C","year":"1993","unstructured":"Antignac C, Arduy CH, Beckmann JS, et al.. A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p. Nat Genet. 1993, 3:342-5. 10.1038\/ng0493-342","journal-title":"Nat Genet"},{"key":"ref19","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/7.5.905","article-title":"Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease","volume":"7","author":"Christodoulou K","year":"1998","unstructured":"Christodoulou K, Tsingis M, Stavrou C, et al.. Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease. Hum Mol Genet. 1998, 7:905-11. 10.1093\/hmg\/7.5.905","journal-title":"Hum Mol Genet"},{"key":"ref20","doi-asserted-by":"publisher","DOI":"10.1111\/j.1523-1755.2002.kid581.x","article-title":"Autosomal-dominant medullary cystic kidney disease type 1: clinical and molecular findings in six large Cypriot families","volume":"62","author":"Stavrou C","year":"2002","unstructured":"Stavrou C, Koptides M, Tombazos C, et al.. Autosomal-dominant medullary cystic kidney disease type 1: clinical and molecular findings in six large Cypriot families. Kidney Int. 2002, 62:1385-94. 10.1111\/j.1523-1755.2002.kid581.x","journal-title":"Kidney Int"},{"key":"ref21","doi-asserted-by":"publisher","DOI":"10.1038\/ng.2543","article-title":"Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing","volume":"45","author":"Kirby A","year":"2013","unstructured":"Kirby A, Gnirke A, Jaffe DB, et al.. Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Nat Genet. 2013, 45:299-303. 10.1038\/ng.2543","journal-title":"Nat Genet"},{"key":"ref22","doi-asserted-by":"publisher","DOI":"10.1093\/ndt\/gfab268","article-title":"Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease","volume":"38","author":"Mabillard H","year":"2023","unstructured":"Mabillard H, Sayer JA, Olinger E. Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease. Nephrol Dial Transplant. 2023, 38:271-82. 10.1093\/ndt\/gfab268","journal-title":"Nephrol Dial Transplant"},{"key":"ref23","doi-asserted-by":"publisher","DOI":"10.1016\/j.kint.2020.04.038","article-title":"Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations\u00a0in UMOD and MUC1","volume":"98","author":"Olinger E","year":"2020","unstructured":"Olinger E, Hofmann P, Kidd K, et al.. Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations\u00a0in UMOD and MUC1. Kidney Int. 2020, 98:717-31. 10.1016\/j.kint.2020.04.038","journal-title":"Kidney Int"},{"key":"ref24","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.c.32008","article-title":"Autosomal dominant tubulointerstitial kidney disease: a review","volume":"190","author":"\u017divn\u00e1 M","year":"2022","unstructured":"\u017divn\u00e1 M, Kidd KO, Bare\u0161ov\u00e1 V, H\u016flkov\u00e1 H, Kmoch S, Bleyer AJ Sr. Autosomal dominant tubulointerstitial kidney disease: a review. Am J Med Genet C Semin Med Genet. 2022, 190:309-24. 10.1002\/ajmg.c.32008","journal-title":"Am J Med Genet C Semin Med Genet"},{"key":"ref25","doi-asserted-by":"publisher","DOI":"10.1038\/s41572-019-0109-9","article-title":"Autosomal dominant tubulointerstitial kidney disease","volume":"5","author":"Devuyst O","year":"2019","unstructured":"Devuyst O, Olinger E, Weber S, Eckardt KU, Kmoch S, Rampoldi L, Bleyer AJ. Autosomal dominant tubulointerstitial kidney disease. Nat Rev Dis Primers. 2019, 5:60. 10.1038\/s41572-019-0109-9","journal-title":"Nat Rev Dis Primers"},{"key":"ref26","doi-asserted-by":"publisher","DOI":"10.1016\/j.kint.2022.04.031","article-title":"Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases","volume":"102","author":"Wopperer FJ","year":"2022","unstructured":"Wopperer FJ, Knaup KX, Stanzick KJ, et al.. Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases. Kidney Int. 2022, 102:405-20. 10.1016\/j.kint.2022.04.031","journal-title":"Kidney Int"},{"key":"ref27","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0175970","article-title":"Mutant uromodulin expression leads to altered homeostasis of the endoplasmic reticulum and activates the unfolded protein response","volume":"12","author":"Schaeffer C","year":"2017","unstructured":"Schaeffer C, Merella S, Pasqualetto E, Lazarevic D, Rampoldi L. Mutant uromodulin expression leads to altered homeostasis of the endoplasmic reticulum and activates the unfolded protein response. PLoS One. 2017, 12:e0175970. 10.1371\/journal.pone.0175970","journal-title":"PLoS One"},{"key":"ref28","doi-asserted-by":"publisher","DOI":"10.1046\/j.1523-1755.2003.00081.x","article-title":"Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene","volume":"64","author":"Bleyer AJ","year":"2003","unstructured":"Bleyer AJ, Woodard AS, Shihabi Z, et al.. Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene. Kidney Int. 2003, 64:36-42. 10.1046\/j.1523-1755.2003.00081.x","journal-title":"Kidney Int"},{"key":"ref29","doi-asserted-by":"publisher","DOI":"10.1007\/s00467-004-1719-2","article-title":"Clinico-pathologic findings in medullary cystic kidney disease type 2","volume":"20","author":"Bleyer AJ","year":"2005","unstructured":"Bleyer AJ, Hart TC, Willingham MC, Iskandar SS, Gorry MC, Trachtman H. Clinico-pathologic findings in medullary cystic kidney disease type 2. Pediatr Nephrol. 2005, 20:824-7. 10.1007\/s00467-004-1719-2","journal-title":"Pediatr Nephrol"},{"key":"ref30","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2009.07.010","article-title":"Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure","volume":"85","author":"Zivn\u00e1 M","year":"2009","unstructured":"Zivn\u00e1 M, H\u016flkov\u00e1 H, Matignon M, et al.. Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure. Am J Hum Genet. 2009, 85:204-13. 10.1016\/j.ajhg.2009.07.010","journal-title":"Am J Hum Genet"},{"key":"ref31","article-title":"Autosomal Dominant Tubulointerstitial Kidney Disease - MUC1","author":"Bleyer AJ","year":"2013","unstructured":"Bleyer AJ, \u017divn\u00e1 M, Kidd K, et al.. Autosomal Dominant Tubulointerstitial Kidney Disease - MUC1. GeneReviews\u00ae . Adam MP, Feldman J, Mirzaa GM, et al. (ed): University of Washington, Seattle, WA; 2013."},{"key":"ref32","doi-asserted-by":"publisher","DOI":"10.1038\/s41598-017-07804-6","article-title":"Early involvement of cellular stress and inflammatory signals in the pathogenesis of tubulointerstitial kidney disease due to UMOD mutations","volume":"7","author":"Trudu M","year":"2017","unstructured":"Trudu M, Schaeffer C, Riba M, et al.. Early involvement of cellular stress and inflammatory signals in the pathogenesis of tubulointerstitial kidney disease due to UMOD mutations. Sci Rep. 2017, 7:7383. 10.1038\/s41598-017-07804-6","journal-title":"Sci Rep"},{"key":"ref33","doi-asserted-by":"publisher","DOI":"10.1038\/srep42970","article-title":"Mitochondrial dysregulation secondary to endoplasmic reticulum stress in autosomal dominant tubulointerstitial kidney disease - UMOD (ADTKD-UMOD)","volume":"7","author":"Kemter E","year":"2017","unstructured":"Kemter E, Fr\u00f6hlich T, Arnold GJ, Wolf E, Wanke R. Mitochondrial dysregulation secondary to endoplasmic reticulum stress in autosomal dominant tubulointerstitial kidney disease - UMOD (ADTKD-UMOD). Sci Rep. 2017, 7:42970. 10.1038\/srep42970","journal-title":"Sci Rep"},{"key":"ref34","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMra2308577","article-title":"Genetics of chronic kidney disease","volume":"391","author":"Vivante A","year":"2024","unstructured":"Vivante A. Genetics of chronic kidney disease. N Engl J Med. 2024, 391:627-39. 10.1056\/NEJMra2308577","journal-title":"N Engl J Med"},{"key":"ref35","doi-asserted-by":"publisher","DOI":"10.1007\/s00467-024-06350-4","article-title":"Case-inspired exploration of renin mutations in autosomal dominant tubulointerstitial kidney disease: not all paths lead to the endoplasmic reticulum","volume":"39","author":"Niedbalska-Tarnowska J","year":"2024","unstructured":"Niedbalska-Tarnowska J, Jakubowska A, Majkowski M, et al.. Case-inspired exploration of renin mutations in autosomal dominant tubulointerstitial kidney disease: not all paths lead to the endoplasmic reticulum. Pediatr Nephrol. 2024, 39:2363-75. 10.1007\/s00467-024-06350-4","journal-title":"Pediatr Nephrol"},{"key":"ref36","doi-asserted-by":"publisher","DOI":"10.1038\/ki.2014.72","article-title":"Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin","volume":"86","author":"Ekici AB","year":"2014","unstructured":"Ekici AB, Hackenbeck T, Morini\u00e8re V, et al.. Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin. Kidney Int. 2014, 86:589-99. 10.1038\/ki.2014.72","journal-title":"Kidney Int"},{"key":"ref37","doi-asserted-by":"publisher","DOI":"10.1016\/j.kint.2020.02.010","article-title":"Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference","volume":"97","author":"Levey AS","year":"2020","unstructured":"Levey AS, Eckardt KU, Dorman NM, et al.. Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference. Kidney Int. 2020, 97:1117-29. 10.1016\/j.kint.2020.02.010","journal-title":"Kidney Int"},{"key":"ref38","doi-asserted-by":"publisher","DOI":"10.1007\/s00467-011-1915-9","article-title":"Acute tubulointerstitial nephritis","volume":"27","author":"Ulinski T","year":"2012","unstructured":"Ulinski T, Sellier-Leclerc AL, Tudorache E, Bensman A, Aoun B. Acute tubulointerstitial nephritis. Pediatr Nephrol. 2012, 27:1051-7. 10.1007\/s00467-011-1915-9","journal-title":"Pediatr Nephrol"},{"key":"ref39","doi-asserted-by":"publisher","DOI":"10.1053\/j.ajkd.2017.08.024","article-title":"Autosomal dominant tubulointerstitial kidney disease due to MUC1 mutation","volume":"71","author":"Yu SM","year":"2018","unstructured":"Yu SM, Bleyer AJ, Anis K, et al.. Autosomal dominant tubulointerstitial kidney disease due to MUC1 mutation. Am J Kidney Dis. 2018, 71:495-500. 10.1053\/j.ajkd.2017.08.024","journal-title":"Am J Kidney Dis"},{"key":"ref40","doi-asserted-by":"publisher","DOI":"10.1681\/ASN.2007121330","article-title":"Improving the recognition of hereditary interstitial kidney disease","volume":"20","author":"Bleyer AJ","year":"2009","unstructured":"Bleyer AJ. Improving the recognition of hereditary interstitial kidney disease. J Am Soc Nephrol. 2009, 20:11-3. 10.1681\/ASN.2007121330","journal-title":"J Am Soc Nephrol"},{"key":"ref41","doi-asserted-by":"publisher","DOI":"10.1053\/j.ajkd.2004.06.027","article-title":"Medullary cystic kidney disease type 1 in a large Native-American kindred","volume":"44(4)","author":"Kiser RL","year":"2004","unstructured":"Kiser RL, Wolf MT, Martin JL, et al.. Medullary cystic kidney disease type 1 in a large Native-American kindred. Am J Kidney Dis. 2004, 44(4):611-7. 10.1053\/j.ajkd.2004.06.027","journal-title":"Am J Kidney Dis"},{"key":"ref42","doi-asserted-by":"publisher","DOI":"10.1038\/ki.2015.28","article-title":"Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus report","volume":"88","author":"Eckardt KU","year":"2015","unstructured":"Eckardt KU, Alper SL, Antignac C, et al.. Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus report. Kidney Int. 2015, 88:676-83. 10.1038\/ki.2015.28","journal-title":"Kidney Int"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/428175-renaming-medullary-cystic-kidney-disease-a-review-of-semantic-nomenclature","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,11,11]],"date-time":"2025-11-11T12:55:22Z","timestamp":1762865722000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/428175-renaming-medullary-cystic-kidney-disease-a-review-of-semantic-nomenclature"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,11,11]]},"references-count":42,"URL":"https:\/\/doi.org\/10.7759\/cureus.96561","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2025,11,11]]}}}