چكيده لاتين :
Mobius Syndrome is rare, heterogeneous and no progressive congenital 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, or facial and limbs anomalies.
The main cause of clinical syndrome is agenesis of cranial nerve nucleus in the pones.
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, no progressive 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 convergence of eyes ant left gaze, divergence of eyes at upward gaze and Goiter of grade two. Para clinical studies such as brain MRI, Echocardiography, ECG, Liver and kidney fuction tests, thyroid hormones and audiometery were normal. NCV Showed axonal type neuropathy of both facial nerves.
