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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Amaltea Medical Publishing House
2018-12-01
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Series: | Romanian Journal of Neurology |
Subjects: | |
Online Access: | https://rjn.com.ro/articles/2018.4/RJN_2018_4_Art-05.pdf |