ABSTRACT
Mobius Syndrome is rare, heterogeneous and nonprogressive congentital disorder that is mostly seen sporadically and has been reported few cases. The principle clinical features of the syndrome are bilateral abducens paresis with different degree, incomplete and bilateral facal nerve paresis, orofacial and limbs anomalies
The main cause of clinical syndrome is agenesis of cranial nerve nucleus in the ponse
Our patient is an 18-Year old man with history of poor sucking, lack of impressions during crawing and bilateral club foot at birth time. His parents noticed disorder of eye movements in the infancy period, these findings had stable, nonprogressive course
Sign that have been found in the clinical assessment are:
Bilateral, peripheral Type facial never paresis more on the left, bilateral club foot, complete inability of conjugated gaze to the right convegence of eyes ant left gaze, divergence of eyes at upward gaze and Goiter of grade two. Paraclinical studies such as brain MRI, Echocardiography, ECG, Liver and kideny fuction tests, thyroid hormones and audiometery were normal. NCV Showed axonal ytpe neuopathy of both facial nerves