In the press: „Rare Diseases depend on correct diagnosis“ – Interview with Assoc. Prof. DI DDr. Kasper in seltenekrankheit.at about Morbus Fabry

ARCHIMEDlife founder Assoc. Prof. DI DDr. David C. Kasper in an interview about the correct diagnosis of Morbus Fabry and the challenges for physicians in detecting this
x-chromosomal inherited disease. (in GERMAN)

A standardized test supports Healthcare Professionals in detecting Morbus Fabry or – even better – to eliminate it quickly from the list of potential diseases, especially when clinical symptoms are unspecific.

 

DDr. Kasper sums up the pros and cons of enzygmatic and genetic testing in male and female patients and underlines the importance of Dried Blood Spots as valuable IVD blood sampling method.

Published on 26th of September 2017 by KURIER Austria (daily press) and Media Planet International, special issue „Seltene Krankheit“, Rare Diseases, in Austria.

 

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