Fabry Disease - literature review
Introduction and objective: Fabry disease (FD) is a rare lysosomal storage disorder that can manifest in classical and atypical forms, with the latter being more common. It results from deficient alpha-galactosidase activity, leading to the accumulation of globotriaosylceramide (Gb3), causing infla...
Saved in:
| Main Authors: | Krystian Wdowiak, Agnieszka Maciocha, Julia Wąż, Aleksandra Witas, Adrian Muzyka, Julia Rydzek, Ewa Gardocka |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Kazimierz Wielki University
2024-11-01
|
| Series: | Journal of Education, Health and Sport |
| Subjects: | |
| Online Access: | https://apcz.umk.pl/JEHS/article/view/56177 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Fabry disease in the haemodialysis population: outcome of a UK screening study (SoFAH)
by: K.P. Ng, et al.
Published: (2025-05-01) -
Modern Approach to Fabry Disease Diagnosis and Management in Children
by: Olga Ya. Smirnova, et al.
Published: (2024-02-01) -
A little bit about sphingolipidoses in cardiology: a clinical case of Fabry disease
by: Artyom A. Vedernikov, et al.
Published: (2025-01-01) -
Clinical and pathological features of 10 cases of Fabry’s disease with renal damage
by: HE Juan, et al.
Published: (2020-01-01) -
Fabry Disease Podocytes Reveal Ferroptosis as a Potential Regulator of Cell Pathology
by: Andrea F. Wise, et al.
Published: (2025-02-01)