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IgA nephritis in a patient with Alagille syndrome and a transplanted liver (1992)

Gilboa, Nisan ; Hopp, Laszlo ; Agostini, Rocco M.

Springer

Pediatric nephrology 6 (1992), S. 559-561

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ISSN: 1432-198X

Keywords: Alagille syndrome ; Arteriohepatic dysplasia ; IgA nephritis ; Liver transplantation ; Cyclosporine A

Source: Springer Online Journal Archives 1860-2000

Topics: Medicine

Notes: Abstract Alagille syndrome (arteriohepatic dysplasia) is a major cause of intrahepatic cholestasis in infancy. The present report describes a patient with Alagille syndrome who presented with hematuria and IgA nephritis 7 years after an orthotopic liver transplantation and immunosuppression. This patient suggests that glomerular lipidosis is not an inherent feature of the Alagille syndrome, and that IgA nephritis may develop in spite of ongoing immunosuppressive treatment.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1007/BF00866506

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