Möbius syndrome is a congenital condition, the etiology when is not associated with misoprostol is not well defined. Signs and symptoms include difficulty swallowing, speech problems, drooling, strabismus, limitation of eye movement and more importantly, the facial blankness that these individuals have, result of the facial paralysis, due to atrophy of the cranial nerves that are involved in this condition. The ability to express emotions is affected and are considered "children without a smile." There is currently no treatment to solvent the birth defects, the treatment options for reduce these alterations is the surgical option that has as main objective to restore muscle function through various techniques, used as required, the possibil...
Introduction: Möbius syndrome is a heterogeneous congenital disorder that is linked to bilateral pal...
Purpose: Long-standing unilateral facial palsy is treated primarily with free-flap surgery using the...
Möbius syndrome is a congenital disease which is characterized by horizontal ophthalmoplegia and fac...
Background: Moebius syndrome, a rare congenital disorder of varying severity, involves multiple cran...
Abstract Background: Moebius syndrome, a rare congenital disorder of varying severity, involves mul...
Objective. To perform a preliminary test of a new rehabilitation treatment (FIT-SAT), based on mirro...
Summary:. Moebius syndrome is a rare congenital facial palsy that can generate serious emotional rep...
BACKGROUND: Craniofacial microsomia is associated with maxillomandibular hypoplasia, microtia, soft-...
Moebius syndrome is a low-prevalence congenital disease characterized by facial paralysis due to inv...
In this article the indications and surgical treatment options for patients with facial nerve palsy ...
Moebius Syndrome (MBS) is a rare disorder, characterized by congenital, non-progressive facial palsy...
Functional and Aesthetic Approach to Adult Unoperated Mo¨bius Syndrome: Orthognathic Surgery follo...
BACKGROUND: Moebius syndrome is a rare condition characterized by bilateral facial and abducens nerv...
Gracilis muscle is the most commonly used muscle in facial paralysis. Although the use of the contra...
Background: Clinical challenges associated with Moebius syndrome, a rare congenital neuromuscular di...
Introduction: Möbius syndrome is a heterogeneous congenital disorder that is linked to bilateral pal...
Purpose: Long-standing unilateral facial palsy is treated primarily with free-flap surgery using the...
Möbius syndrome is a congenital disease which is characterized by horizontal ophthalmoplegia and fac...
Background: Moebius syndrome, a rare congenital disorder of varying severity, involves multiple cran...
Abstract Background: Moebius syndrome, a rare congenital disorder of varying severity, involves mul...
Objective. To perform a preliminary test of a new rehabilitation treatment (FIT-SAT), based on mirro...
Summary:. Moebius syndrome is a rare congenital facial palsy that can generate serious emotional rep...
BACKGROUND: Craniofacial microsomia is associated with maxillomandibular hypoplasia, microtia, soft-...
Moebius syndrome is a low-prevalence congenital disease characterized by facial paralysis due to inv...
In this article the indications and surgical treatment options for patients with facial nerve palsy ...
Moebius Syndrome (MBS) is a rare disorder, characterized by congenital, non-progressive facial palsy...
Functional and Aesthetic Approach to Adult Unoperated Mo¨bius Syndrome: Orthognathic Surgery follo...
BACKGROUND: Moebius syndrome is a rare condition characterized by bilateral facial and abducens nerv...
Gracilis muscle is the most commonly used muscle in facial paralysis. Although the use of the contra...
Background: Clinical challenges associated with Moebius syndrome, a rare congenital neuromuscular di...
Introduction: Möbius syndrome is a heterogeneous congenital disorder that is linked to bilateral pal...
Purpose: Long-standing unilateral facial palsy is treated primarily with free-flap surgery using the...
Möbius syndrome is a congenital disease which is characterized by horizontal ophthalmoplegia and fac...