mirror movements 2
An autosomal dominant (OMIM:614508) condition with incomplete penetration, characterised by mirror movements*, especially in the upper limbs, that persist beyond age 10.
*Involuntary movements of a side of the body that mirror intentional movements on the opposite side
Molecular pathology Defects in RAD51, which encodes a recombinase involved in homologous recombination and DNA repair, cause mirror movements 2..
JIACM 2002; 3(2): 177-81