Complement-mediated thrombotic microangiopathy on a background of Alport syndrome: a case report

Craig Peter Coorey; Theo de Malmanche; Angela Chou; Martin Feddersen

doi:10.1111/nep.14305

Complement-mediated thrombotic microangiopathy on a background of Alport syndrome: a case report

Craig Peter Coorey, Theo de Malmanche, Angela Chou, Martin Feddersen

School of Medicine

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Abstract

Here we present a case of complement-mediated thrombotic microangiopathy (TMA) in a patient who has a background of Stage 5 chronic kidney disease secondary to Alport syndrome. We explain our approach to the diagnosis of TMA, especially the reliance on non-renal manifestations of TMA and the role of kidney biopsy given there was a background of advanced kidney impairment at baseline.

Original language	English
Pages (from-to)	688-690
Number of pages	3
Journal	Nephrology
Volume	29
Issue number	10
DOIs	https://doi.org/10.1111/nep.14305
Publication status	Published - 2024

Bibliographical note

Publisher Copyright:
© 2024 The Authors. Nephrology published by John Wiley & Sons Australia, Ltd on behalf of Asian Pacific Society of Nephrology.

Keywords

acute kidney injury
Alport syndrome (hereditary nephritis)
thrombotic microangiopathy

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1111/nep.14305Licence: CC BY-NC-ND

Full textFinal published version, 698 KBLicence: CC BY-NC-ND

Cite this

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Complement-mediated thrombotic microangiopathy on a background of Alport syndrome: a case report

Abstract

Bibliographical note

Keywords

UN SDGs

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