Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome | Zendy

ErnestH. Shaw | Zendy; D. Colville | Zendy; Y. Y. Wang | Zendy; Kewei Zhang | Zendy; Hayat Dagher | Zendy; R. G. Fassett | Zendy; Robyn H. Guymer | Zendy; Judy Savige | Zendy

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Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome

Author(s) -

ErnestH. Shaw,

D. Colville,

Y. Y. Wang,

Kewei Zhang,

Hayat Dagher,

R. G. Fassett,

Robyn H. Guymer,

Judy Savige

Publication year - 2006

Publication title -

nephrology dialysis transplantation

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.654

H-Index - 168

eISSN - 1460-2385

pISSN - 0931-0509

DOI - 10.1093/ndt/gfl607

Subject(s) - alport syndrome , medicine , retinopathy , glomerulonephritis , kidney disease , pathology , dermatology , ophthalmology , kidney , diabetes mellitus , endocrinology

Alport syndrome is an inherited disease resulting in kidney failure, hearing loss and ocular abnormalities. Alport syndrome is however often unrecognized, and the aim of this study was to characterize the associated but rarely described peripheral retinopathy and determine whether its demonstration was diagnostically helpful.

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