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Rare features associated with Mobius syndrome: Report of two cases

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...

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Autores principales: Ghosh, Rumela, Shetty, Vikram, Hegde, Shruthi, Babu, G Subhas, Ajila, Vidya, Kishore P, Nanda, Nair, Mithula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390129/
https://www.ncbi.nlm.nih.gov/pubmed/28413599
http://dx.doi.org/10.15171/joddd.2017.012
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author Ghosh, Rumela
Shetty, Vikram
Hegde, Shruthi
Babu, G Subhas
Ajila, Vidya
Kishore P, Nanda
Nair, Mithula
author_facet Ghosh, Rumela
Shetty, Vikram
Hegde, Shruthi
Babu, G Subhas
Ajila, Vidya
Kishore P, Nanda
Nair, Mithula
author_sort Ghosh, Rumela
collection PubMed
description 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.
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spelling pubmed-53901292017-04-14 Rare features associated with Mobius syndrome: Report of two cases Ghosh, Rumela Shetty, Vikram Hegde, Shruthi Babu, G Subhas Ajila, Vidya Kishore P, Nanda Nair, Mithula J Dent Res Dent Clin Dent Prospects Case Report 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. Tabriz University of Medical Sciences 2017 2017-03-15 /pmc/articles/PMC5390129/ /pubmed/28413599 http://dx.doi.org/10.15171/joddd.2017.012 Text en © 2017 Ghosh et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article published and distributed by Tabriz University of Medical Sciences under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ghosh, Rumela
Shetty, Vikram
Hegde, Shruthi
Babu, G Subhas
Ajila, Vidya
Kishore P, Nanda
Nair, Mithula
Rare features associated with Mobius syndrome: Report of two cases
title Rare features associated with Mobius syndrome: Report of two cases
title_full Rare features associated with Mobius syndrome: Report of two cases
title_fullStr Rare features associated with Mobius syndrome: Report of two cases
title_full_unstemmed Rare features associated with Mobius syndrome: Report of two cases
title_short Rare features associated with Mobius syndrome: Report of two cases
title_sort rare features associated with mobius syndrome: report of two cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390129/
https://www.ncbi.nlm.nih.gov/pubmed/28413599
http://dx.doi.org/10.15171/joddd.2017.012
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