Moebius Syndrome: What We Know So Far
- PMID: 36960250
- PMCID: PMC10030064
- DOI: 10.7759/cureus.35187
Moebius Syndrome: What We Know So Far
Abstract
Moebius syndrome (MBS) is a rare congenital cranial nerve disorder characterized by unilateral, bilateral symmetrical, or asymmetrical facial (VII) and abducens (VI) nerve palsies. Genetics and rhombencephalon vascular disturbances from intrauterine environmental exposures have been attributed to its development. It can present with various orofacial abnormalities. Although the diagnosis is purely clinical, certain characteristic features are present in the brain's images. With no cure, it is essential to devise management on a personalized basis. We discuss etiology, presentation, diagnostic approaches, and effective management in the existing literature. This comprehensive review examines the clinic-pathological aspects of Moebius syndrome. The authors employed the PUBMED base index to identify pertinent literature and reference it according to research keywords. Findings suggest the most popular etiology is the theory of intrauterine vascular disruption to the brainstem during embryogenesis, followed by the genetic hypothesis. Intrauterine environmental exposures have been implicated as potential risk factors. Facial and abducens nerve palsies are the most common presenting features. However, clinical manifestations of lower cranial nerves (IX, X, XI, XII) may be present with orthopedic anomalies and intellectual deficiencies. The diagnosis is clinical with minimal defined diagnostic criteria. Characteristic radiological manifestations involving the brainstem and cerebellum can be observed in imaging studies. With no definitive treatment options, a multidisciplinary approach is employed to provide supportive care. Despite radiological manifestations, Moebius syndrome is diagnosed clinically. Although incurable, a multidisciplinary approach, with personalized rehabilitative measures, can manage physical and psychological deficits; however, standard guidelines need to be established.
Keywords: congenital ophthalmoplegia and facial paresis; moebius congenital oculofacial paralysis; moebius sequence; moebius spectrum; moebius syndrome.
Copyright © 2023, Zaidi et al.
Conflict of interest statement
The authors have declared that no competing interests exist.
References
-
- The faces of Moebius syndrome: recognition and anticipatory guidance. Broussard AB, Borazjani JG. MCN Am J Matern Child Nurs. 2008;33:272–278. - PubMed
-
- Moebius syndrome: clinical features, diagnosis, management and early intervention. Picciolini O, Porro M, Cattaneo E, Castelletti S, Masera G, Mosca F, Bedeschi MF. http://ttps://pubmed.ncbi.nlm.nih.gov/27260152/ Ital J Pediatr. 2016;42:56. - PMC - PubMed
-
- Moebius syndrome. Kumar D. https://pubmed.ncbi.nlm.nih.gov/2319579/ J Med Genet. 1990;27:122–126. - PMC - PubMed
-
- Magnetic resonance imaging findings in sporadic Möbius syndrome. Wu SQ, Man FY, Jiao YH, Xian JF, Wang YD, Wang ZC. https://pubmed.ncbi.nlm.nih.gov/23786943/ Chin Med J (Engl) 2013;126:2304–2307. - PubMed
-
- Group III Möbius syndrome: CT and MR findings. Kuhn MJ, Clark HB, Morales A, Shekar PC. https://pubmed.ncbi.nlm.nih.gov/2120994/ AJNR Am J Neuroradiol. 1990;11:903–904. - PMC - PubMed
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