薄基底膜病变不仅仅是IV型胶原肾病：不要低估胶原蛋白的“修饰”添加物。 - Suppr

Thin basement membrane lesion is not only a collagen IV nephropathy: do not underestimate "decorative" additions to collagens.

作者信息

Deltas Constantinos

机构信息

University of Cyprus Medical School, University of Cyprus, Nicosia, Cyprus; Center of Excellence in Biobanking and Biomedical Research, biobank.cy, Nicosia, Cyprus.

出版信息

Kidney Int. 2022 Dec;102(6):1203-1205. doi: 10.1016/j.kint.2022.08.014. Epub 2022 Aug 27.

DOI:10.1016/j.kint.2022.08.014

PMID:36041560

Abstract

摘要

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Thin basement membrane lesion is not only a collagen IV nephropathy: do not underestimate "decorative" additions to collagens.薄基底膜病变不仅仅是IV型胶原肾病：不要低估胶原蛋白的“修饰”添加物。

Kidney Int. 2022 Dec;102(6):1203-1205. doi: 10.1016/j.kint.2022.08.014. Epub 2022 Aug 27.

Alport syndrome and thin basement membrane nephropathy: unraveling the tangled strands of type IV collagen.奥尔波特综合征与薄基底膜肾病：解开IV型胶原的纠结线索

Kidney Int. 2004 Mar;65(3):1109-10. doi: 10.1111/j.1523-1755.2004.00570.x.

[Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].[IV型胶原肾病：从薄基底膜肾病到Alport综合征]

Orv Hetil. 2005 Dec 25;146(52):2647-53.

Slowly Progressive Male Alport Syndrome Evaluated by Serial Biopsy: Importance of Type IV Collagen Staining.通过连续活检评估的缓慢进展性男性奥尔波特综合征：IV型胶原染色的重要性

Intern Med. 2022 Apr 15;61(8):1205-1209. doi: 10.2169/internalmedicine.7372-21. Epub 2021 Oct 12.

Spectrum of collagen type IV nephropathies: from thin basement membrane nephropathy to Alport syndrome.IV型胶原肾病谱：从薄基底膜肾病到Alport综合征。

Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:323-6. doi: 10.2298/sarh08s4323v.

Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis.奥尔波特综合征与薄肾小球基底膜肾病：诊断的实用方法

Arch Pathol Lab Med. 2009 Feb;133(2):224-32. doi: 10.5858/133.2.224.

Familial hematuric syndromes--Alport syndrome, thin glomerular basement membrane disease and Fechtner/Epstein syndromes.家族性血尿综合征——阿尔波特综合征、薄肾小球基底膜病以及费希特纳/爱泼斯坦综合征。

Contrib Nephrol. 2001(136):79-99. doi: 10.1159/000060181.

Approach to the diagnosis of thin basement membrane nephropathy in females with the use of antibodies to type IV collagen.使用IV型胶原抗体诊断女性薄基底膜肾病的方法

Arch Pathol Lab Med. 2001 May;125(5):631-6. doi: 10.5858/2001-125-0631-ATTDOT.

Collagen IV diseases: A focus on the glomerular basement membrane in Alport syndrome.IV型胶原疾病：聚焦于Alport综合征中的肾小球基底膜。

Matrix Biol. 2017 Jan;57-58:45-54. doi: 10.1016/j.matbio.2016.08.005. Epub 2016 Aug 27.

Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.IV型胶原肾病的常染色体显性遗传形式存在于临床病理诊断困难的遗传性肾炎患者中。

Nephrology (Carlton). 2018 Oct;23(10):940-947. doi: 10.1111/nep.13115.

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A nonsense mutation in the Tripartite motif containing 8 (TRIM8) gene, mimicking collagenopathy.含三联基序蛋白8（TRIM8）基因中的无义突变，类似于胶原病。

Pediatr Nephrol. 2025 May;40(5):1579-1581. doi: 10.1007/s00467-024-06636-7. Epub 2024 Dec 21.

Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice.人类和小鼠中孟德尔单基因胶原 IV 肾病的遗传修饰物。

Genes (Basel). 2023 Aug 25;14(9):1686. doi: 10.3390/genes14091686.

Novel and Founder Pathogenic Variants in X-Linked Alport Syndrome Families in Greece.希腊 X 连锁 Alport 综合征家系中的新型和创始致病性变异。

Genes (Basel). 2022 Nov 24;13(12):2203. doi: 10.3390/genes13122203.

A Comparative Presentation of Mouse Models That Recapitulate Most Features of Alport Syndrome.重现 Alport 综合征大部分特征的小鼠模型的比较介绍。

Genes (Basel). 2022 Oct 18;13(10):1893. doi: 10.3390/genes13101893.

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Thin basement membrane lesion is not only a collagen IV nephropathy: do not underestimate "decorative" additions to collagens.

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