Fabry Disease

Fabry disease is a rare genetic disease involving a deficiency of an enzyme. A decrease in the enzyme activity leads to a selective suffering of specific anatomic and functional structures resulting in heteromorphic clinical signs that increase the difficulty of early diagnosis. Knowing and identify...

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Bibliographic Details
Main Authors: Ioana Simina Barac, Doru Flaviu Tomesc, Adina Stan, Vitalie Vacaras, Fior Dafin Muresanu
Format: Article
Language:English
Published: Amaltea Medical Publishing House 2018-12-01
Series:Romanian Journal of Neurology
Subjects:
Online Access:https://rjn.com.ro/articles/2018.4/RJN_2018_4_Art-05.pdf