- Open Access
Erratum to: Effectiveness of agalsidase alfa enzyme replacement in Fabry disease: cardiac outcomes after 10 years’ treatment
© The Author(s). 2016
- Received: 6 July 2016
- Accepted: 6 July 2016
- Published: 12 July 2016
The original article was published in Orphanet Journal of Rare Diseases 2015 10:125
Following the publication of our article “Effectiveness of agalsidase alfa enzyme replacement in Fabry disease: cardiac outcomes after 10 years’ treatment” by Kampmann et al.  we have become aware that the dose of agalsidase alfa was not reported.
Eligible patients had a Fabry disease diagnosis confirmed by enzyme assay (males) and/or DNA analysis (males and females), were aged ≥14 years at treatment start, and had received agalsidase alfa (Replagal®; Shire, Lexington, Massachusetts, USA) ERT at a dose of 0.2 mg/kg body weight every other week for approximately 10 years.
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