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Fabry EM

Chris Larsen, MD renal pathologist at arkana laboratories
By Chris Larsen, MD

Jun 01, 2017

Fabry EM

Electron photomicrograph of a glomerular podocyte showing the characteristic electron dense laminated inclusions of Fabry disease. Fabry is a lysosomal storage disease with X-linked inheritance. Mutations in the gene for the enzyme alpha galactosidase A (GLA) result in accumulation of a glycolipid known as globotriaosylceramide (GL-3) in tissues including the kidney.


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