Abstract
Mobius syndrome is a rare congenital disorder with the preliminary diagnostic criteria of congenital facial and abducent nerve palsy. Involvement of other cranial nerves, too, is common. Prevalence rate of this syndrome is approximately 1 in 100,000 neonates. It is of unknown etiology with sporadic occurrence. However, data regarding the occurrence rate in India is limited. Features such as orofacial malformations, limb defects, and musculoskeletal, behavioral, and cognitive abnormalities might be associated. A thorough evaluation to identify the condition and establishing an adequate treatment plan is of utmost important in this condition. We are reporting clinical and radiographic features of Mobius syndrome in two cases along with unusual findings of limb and neck deformity.
Highlights
Mobius syndrome is a congenital facial weakness combined with abnormal ocular abduction in most studies
Based on history given by the patient and features shown on clinical examination, the case was diagnosed as Mobius syndrome
In congenital facial muscular atrophy, positive family history and prenatal or postnatal trauma are generally present, which were not reported in our cases
Summary
Mobius syndrome is a congenital facial weakness combined with abnormal ocular abduction in most studies. We are reporting clinical and radiographic features of Mobius syndrome in two cases along with unusual findings of limb and neck deformity.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of dental research, dental clinics, dental prospects
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.