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名词信息
中 文 名:
先天性肾单位减少伴代偿肥大
英 文 名:
oligomeganephronia
中文又称:
肾单位稀少巨大症
中文曾称:
名词来源:
所属专业:
肾内科
所属类别:
疾病诊断名词
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Pubmed相关的文献
oligomeganephronia
相关文献:
A Case Report and Literature Review of Oligomeganephronia.
Wang XH, Pan L, He S, Kong DL, Wang W.
Front Med (Lausanne). 2022 Mar 22;9:811992. doi: 10.3389/fmed.2022.811992. eCollection 2022.
PMID:35391889
Clinical and pathological investigation of oligomeganephronia.
Kitakado H, Horinouchi T, Masuda C, Kondo A, Nagai S, Aoto Y, Sakakibara N, Ninchoji T, Yoshikawa N, Nozu K.
Pediatr Nephrol. 2023 Mar;38(3):757-762. doi: 10.1007/s00467-022-05687-y. Epub 2022 Jul 21.
PMID:35861872
A novel pathogenic variant c.262delA in PBX1 causing oligomeganephronia identified using whole-exome sequencing and a literature review.
Hu J, Yang H, Wang X, Ding J, Liao P, Zhu G, Qi C.
Am J Med Genet A. 2023 Dec;191(12):2850-2855. doi: 10.1002/ajmg.a.63364. Epub 2023 Aug 12.
PMID:37571997
Oligomeganephronia in Wolf-Hirschhorn Syndrome.
Sakallioglu O, Gok F.
Indian Pediatr. 2006 Oct;43(10):923-4.
PMID:17079842
Oligomeganephronia: case report and literature review.
Yang XD, Shi W, Li D, Peng T.
Srp Arh Celok Lek. 2014 Nov-Dec;142(11-12):732-5. doi: 10.2298/sarh1412732y.
PMID:25731007
Oligomeganephronia with PAX2 gene deletion diagnosed at the third renal biopsy: a case report.
Yokoyama T, Sakumura N, Inoue N, Ohta K, Wada T.
J Nephrol. 2024 Mar;37(2):495-499. doi: 10.1007/s40620-023-01816-4. Epub 2023 Dec 7.
PMID:38060109
PAX2 Mutation-Related Oligomeganephronia in a Young Adult Patient.
Bitó L, Kalmár T, Maróti Z, Turkevi-Nagy S, Bereczki C, Iványi B.
Case Rep Nephrol Dial. 2020 Nov 30;10(3):163-173. doi: 10.1159/000510841. eCollection 2020 Sep-Dec.
PMID:33363218
PAX2 mutations in oligomeganephronia.
Salomon R, Tellier AL, Attie-Bitach T, Amiel J, Vekemans M, Lyonnet S, Dureau P, Niaudet P, Gubler MC, Broyer M.
Kidney Int. 2001 Feb;59(2):457-62. doi: 10.1046/j.1523-1755.2001.059002457.x.
PMID:11168927
Pathological and clinical characteristics of late-onset oligomeganephronia based on a histomorphometric study.
Ren YL, Li Y, Gao J, Zhou XJ, Yang L, Wang SX.
BMC Nephrol. 2023 Mar 15;24(1):54. doi: 10.1186/s12882-023-03096-3.
PMID:36922764
Oligomeganephronia associated with 4p deletion type chromosomal anomaly.
Park SH, Chi JG.
Pediatr Pathol. 1993 Nov-Dec;13(6):731-40. doi: 10.3109/15513819309048260.
PMID:8108293
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