Related Experiment Video
Updated: Oct 13, 2025

In Vitro Enzyme Measurement to Test Pharmacological Chaperone Responsiveness in Fabry and Pompe Disease
Published on: December 20, 2017
Fabry Disease: A Atypical Presentation
Cláudia Ferreira Tátá1, Margarida Massas1, Filipa Pinto2
1Internal Medicine, Hospital do Espírito Santo de Évora, Évora, PRT.
Fabry Disease (FD), a rare genetic disorder, presents diagnostic challenges due to varied symptoms. This case highlights a non-classical presentation in a 59-year-old man, emphasizing the need for timely diagnosis.
Area of Science:
- Genetics
- Biochemistry
- Neurology
Background:
- Fabry Disease (FD) is a rare X-linked recessive lysosomal storage disorder.
- Caused by GLA gene mutations, it results in deficient alpha-galactosidase A activity.
- FD affects multiple organs and presents with diverse clinical manifestations.
More Related Videos
Related Concept Videos
Chronic Kidney Disease II: Clinical Manifestations
Atherosclerosis II: Clinical Manifestations and Diagnostic Tests
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation
Coronary Artery Disease III: Clinical Manifestations
Lysosomal Hydrolases

