Rare Diseases in Neurology — Caring for a Patient with Pompe’s Disease
Introduction. Pompe disease, a severe metabolic myopathy, is caused by mutations in the gene coding for acid alpha-glucosidase (GAA), what lead to intralysosomal accumulation of glycogen in all tissues, most notably in skeletal muscles. Pompe disease was the first documented lysosomal storage diseas...
Saved in:
| Main Authors: | Anna Roszmann, Mikołaj Hamerski, Marcelina Skrzypek-Czerko |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Państwowa Akademia Nauk Stosowanych we Włocławku
2019-06-01
|
| Series: | Pielęgniarstwo Neurologiczne i Neurochirurgiczne |
| Subjects: | |
| Online Access: | https://apcz.umk.pl/PNIN/article/view/38040 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Results of orthodontic procedure in a patient with classic infantile Pompe disease
by: Carla Maria Grimaldi, et al.
Published: (2025-07-01) -
Five-Year Outcomes of Patients with Pompe Disease Identified by the Pennsylvania Newborn Screen
by: Hayley A. Ron, et al.
Published: (2025-02-01) -
Clinical examination of patients with late-onset Pompe disease: typical and not typical symptoms and signs
by: S. S. Nikitin
Published: (2020-01-01) -
A case of Pompe disease in infant
by: E. F. Sudorgina, et al.
Published: (2015-02-01) -
Pompe disease and ophthalmopathy: literature review
by: Tuy Nga Brignol, et al.
Published: (2015-05-01)