Mobius syndrome is a congenital disorder of facial diplegia associated with
lateral gaze paralysis. Although palsy of the sixth and seventh cranial ne
rves is the minimum diagnostic finding for Mobius syndrome, neuropathologic
evidence indicates that this is a more complex syndrome.(1) Clinically, it
is characterized by a total absence of facial expression and severe esotro
pia, Other anomalies may be associated with this syndrome, especially other
cranial nerve palsies and Poland syndrome, The etiology of this syndrome h
as not been clearly established. Brain stem necrosis resulting from a vascu
lar deficiency has been offered as a possible pathogenetic explanation.(2)
The strabismus in Mobius syndrome is congenital esotropia with bilateral li
mitation in abduction, Even though many reports have described the various
features of Mobius syndrome, only a few articles have reported the results
of strabismus surgery in children, including bimedial rectus muscle recessi
on.(3-5) Some authors report that bilateral medial rectus muscle recession
alone has been disappointing; therefore, a combination of a medial rectus m
uscle recession and a lateral rectus muscle resection was recommended for s
atisfactory results.(5-7) In more severe cases, muscle transposition was ne
eded to ensure straight position of the eyes in primary gaze.(8,9)