The first detailed description of congenital facial paralysis was reported
by Moebius in 1888. It is characterized by either unilateral or bilateral p
aralysis of the facial muscles and an associated abducens palsy. The presen
t report is of two patients with Moebius syndrome, who were also diagnosed
with trismus at birth. Each patient also demonstrated bilateral hypertrophy
of the coronoid process of the mandible. In effect, the zygoma obstructed
the excursion of the mandible because of a "coronoid block." A three-dimens
ional computed tomography scan demonstrated normal temporomandibular joints
but bilateral hypertrophy of the coronoid processes and micrognathia. Both
patients demonstrated less than 10 mm of oral excursion. Bilateral coronoi
dectomies were performed through an intraoral approach. The oral excursions
after surgery increased to at least 20 mm. In each of these patients, the
coronoid process was enlarged relative to the zygoma, which was of normal s
ize and configuration. The trismus was associated with blocking of the coro
noid by the anterior zygoma, preventing open or full excursion of the hypop
lastic mandibles. Moebius syndrome can have a variable presentation at birt
h. In two patients, the authors describe a new finding of hypertrophy of th
e coronoid process and trismus secondary to obstruction of the coronoid by
the hypertrophic zygomas during oral excursions. Each patient is described,
and a review of the literature is discussed.