Literature DB >> 21141008

Alport syndrome.

P Karki1, J K Shrestha.   

Abstract

Alport syndrome is an oculo-renal syndrome characterized by a triad of clinical findings consisting of hemorrhagic nephritis, sensorineural hearing loss and characteristic ocular findings. We report a young male patient who presented with painless diminution of vision associated with hearing loss. The importance of ophthalmic evaluation for suspecting the disease is highlighted.

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Year:  2009        PMID: 21141008     DOI: 10.3126/nepjoph.v1i2.3690

Source DB:  PubMed          Journal:  Nepal J Ophthalmol        ISSN: 2072-6805


  4 in total

1.  Self-Assembled Peptide-Based Biocomposites for Near-Infrared Light Triggered Drug Release to Tumor Cells.

Authors:  Rachel E Daso; Ipsita A Banerjee
Journal:  Biotechnol J       Date:  2020-09-15       Impact factor: 4.677

2.  The Accumulation of VEGFA in the Glomerular Basement Membrane and Its Relationship with Podocyte Injury and Proteinuria in Alport Syndrome.

Authors:  Haiyan Wang; Zhihui Yue; Jinlang Wu; Ting Liu; Ying Mo; Xiaoyun Jiang; Liangzhong Sun
Journal:  PLoS One       Date:  2015-08-14       Impact factor: 3.240

3.  Compound Mutations of the COL4A3 including a Novel Allele Identified in a Patient with Alport Syndrome.

Authors:  Zhendong Wang; Baichun Jiang; Shiqi Jin; Zhao Hu; Guangyi Liu
Journal:  Biomed Res Int       Date:  2020-11-11       Impact factor: 3.411

Review 4.  Ocular Manifestations and Potential Treatments of Alport Syndrome: A Systematic Review.

Authors:  Rahul Ramakrishnan; Atira Shenoy; Damon Meyer
Journal:  J Ophthalmol       Date:  2022-09-08       Impact factor: 1.974

  4 in total

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