Article

A Case Study of Fabry Nephropathy and Its Progression: The First Reported Case in Malaysia

2021-02-25

Abstract excerpt

<title>Abstract</title> <p><bold>Introduction</bold>Fabry disease (FD) is a rare metabolic disorder caused by the genetic deficiency of the lysosomal hydrolase alpha-galactosidase A, causing common and serious kidney complications. We report the first case of Fabry disease detected in Malaysia. <bold>Clinical Scenario</bold>A 35-year-old man had an incidental finding of proteinuria during routine health screening...

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Literature Corpus work: 38b54d65-5175-5e51-af10-c19d723a067b
DOI: 10.21203/rs.3.rs-230368/v1

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