E74.0
Conditions
Interventions
Group 1: Pompe Patients
All participants will be undergo the same study protocol six times at intervals of 3-4 months. An examination day will include written inform content, questionnaires to obtain
Sponsors
BG UK Bergmannsheil / Neurologie
Eligibility
Sex/Gender
All
Age
16 Years to 100 Years
Inclusion criteria
Inclusion criteria: Ensured diagnosis of Morbus Pompe OR no neuromuscular disorders at all (healthy controls)
Exclusion criteria
Exclusion criteria: MR contraindications e.g. implants, respiratory insufficency
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| i)After finishing acquisition and evaluation of all participants for timepoint 1, we will perform initial cross sectional comparisons between LOPD patients and matched controls to reproduce our previous findings, of increased diffusivity in LOPD muscles with <10% fat. ii)After finishing all acquisitions longitudinal analysis of quantitative parameters (diffusion, fat and T2) in LOPD patients and in controls, and the analysis of the interaction between the timespan and the population group will be performed | — |
Countries
Germany
Contacts
Public ContactLara Schlaffke
BG UK Bergmannsheil / Neurologie
Outcome results
None listed