Previous Page  9 / 10 Next Page
Information
Show Menu
Previous Page 9 / 10 Next Page
Page Background

Page 54

Notes:

conferenceseries

.com

Volume 6, Issue 4(Suppl)

OMICS J Radiol, an open access journal

ISSN: 2167-7964

Medical Imaging and Clinical Research 2017

September 11-12, 2017

September 11-12, 2017 | Paris, France

2

nd

World Congress on

Medical Imaging and Clinical Research

Magnetic resonance imaging and post-processing analysis of flexor muscle in Pompe disease

Ala Khasawneh

University of Pécs, Hungary

P

ompe disease is a rare multisystem genetic disorder that is characterized by a deficiency of the lysosomal enzyme acid alpha-

glucosidase and cytoplasmic glycogen accumulation causing damage that leads to muscle weakness. The aim of this study was

to evaluate the muscle MRI pattern of 12 adults with late onset Pompe patients and 12 sex-and age-matched healthy controls (Age

range 19-59). A training procedure was implemented using an exercise dynamometer device; MRI data was used to compare the three

flexor muscles in the lower limb function. MRI data of biceps femoris (BF) muscle, semitendinosus (ST) muscle, semimembranosus

(SM) muscle in exercises over time (base, 30 min, 24 hours) was measured. We performed and quantified T2-weighted (T2-w) data

of flexor muscles, all data were analyzed by using repeated measure ANOVA. According to our results, significantly lower T2 value in

the ST muscle of controls was observed (base=43 ms, 30 min=48 ms, 24 h=43 ms; P<0.05) compared to the patients, but the change

in SM muscle and BF muscle were not significant. In patients, we detected significantly higher T2 value in SM muscle change over

time (base=129 ms, 30 min=132 ms, 24 h=128 ms; P<0.05) compared to the controls, but ST muscle and BF muscle doesn't show

significant change. As a conclusion, we can say that in Pompe patients, the SM muscle can only react to the exercise apparently and

shows us an activity in affected muscle cells, compared to the control SM muscle that does not show any activity that means perhaps

the Pompe disease change the muscle cells structure to interact to the exercise.

Biography

Ala Khasawneh is a Jordanian Doctor. He completed his Diploma in General Medicine (MD) and has been awarded the qualification of a Physician and title of

Doctor of Medicine from National Pirogov Memorial Medical University. He worked in Basma Hospital, Jordan. Currently, he is a PhD fellow in Diagnostic Medical

Imaging in Hungary. As a Doctor, his main interest is to create new pathways for improving health care.

alaakhalel@aol.com

Ala Khasawneh, OMICS J Radiol 2017, 6:4(Suppl)

DOI: 10.4172/2167-7964-C1-013