Mirror movements are involuntary, symmetrical and simultaneous movements occurring on one side of the body that accompany controlateral voluntary movements. Congenital mirror movements (CMM) are characterized by childhood onset and the absence of additional manifestations. The aim of this study is to unravel the pathophysiology of the CMM that remains poorly elucidated. The combination of imaging studies and neurophysiological studies using transcranial magnetic stimulation in a homogeneous and relatively large group of patient is likely to allow us to better understand the underlying pathophysiology of the disorder. Using a linkage analysis approach we will try to identify a locus associated with CMM and related candidate genes.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
40
morphological and functional brain MRI; transcranial magnetic stimulation
morphological and functional brain MRI; transcranial magnetic stimulation
morphological and functional brain MRI; transcranial magnetic stimulation
Fédération des Maladies du Système Nerveux, Hôpital Pitié Salpétrière
Paris, France
- To unravel the pathophysiology of congenital mirror movements - To identify a locus and candidate genes associated with CMM
Time frame: 08/2011
- To study patients with Kallmann syndrome and associated MM based on the same methods and hypothesis
Time frame: 08/2011
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