Previous Page  19 / 38 Next Page
Information
Show Menu
Previous Page 19 / 38 Next Page
Page Background

conferenceseries

.com

Notes:

Volume 6, Issue 4 (Suppl)

J Spine, an open access journal

ISSN: 2165-7939

Page 49

July 24-26, 2017 Rome, Italy

&

Spine and Spinal Disorders

2

nd

International Conference on

Neurology and Neuromuscular Diseases

6

th

International Conference on

CO-ORGANIZED EVENT

Central nervous system involvement in mitochondrial disorders

Josef Finsterer

Veterinary University of Vienna, Austria

Statement of the Problem:

Central nervous system (CNS) disease is increasingly recognized as a manifestation of mitochondrial

disorders (MIDs). However, the broad range of clinical CNS manifestation is still underestimated. This review aims at summarizing

and discussing previous and recent findings concerning the cerebral manifestations of MIDs.

Methodology &Theoretical Orientation:

MIDs literature review was conducted.

Findings:

MIDs frequently present as mitochondrial multiorgan disorder syndrome (MIMODS) either already at onset or later in

the course. After the muscle, the brain is the second most organ which is frequently affected in MIMODS. Cerebral manifestations

of MIDs are variable and may present with or without a lesion on imaging or functional studies but there can be imaging/functional

lesions without clinical manifestations. The most well-known cerebral manifestations of MIDs include stroke-like episodes, epilepsy,

headache, ataxia, movement disorders, hypopituitarism, muscle weakness, psychiatric abnormalities, nystagmus, white and grey

matter lesions, atrophy, basal ganglia calcification, and hypometabolism on FDG-PET. For most of the MIDs only symptomatic

therapy is currently available. Symptomatic treatment should be supplemented by vitamins, co-factors, and antioxidants.

Conclusion & Significance:

Cerebral manifestations of MIDs need to be recognized and appropriately managed since they strongly

determine the outcome of MID patients.

Biography

Josef Finsterer received his MD and is a Professor of Neurology from the University of Vienna, Austria. Since his training as a Clinical Neurologist and

Electrophysiologist at the Neurological Krankenhaus Rosenhuegel and the Ludwig Boltzmann Institute for Epilepsy and Neuromuscular Disorders, he is involved

in the management of neuromuscular disorders, particularly muscular dystrophies and metabolic myopathies. In addition to neuromuscular disorders, research

interests focus on genetics, orphan diseases, and cardiac involvement in genetic conditions.

fifigs1@yahoo.de

Josef Finsterer, J Spine 2017, 6:4(Suppl)

DOI: 10.4172/2165-7939-C1-005