Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence

Möbius syndrome is a rare congenital disorder presenting with facial diplegia and horizontal gaze disturbance. Patients can have additional cranial nerve palsies and musculoskeletal deformities. Neurofibromatosis Type 1 is an uncommon neurocutaneous disorder. The only plausible link between these tw...

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Autores principales: Sharma, Ankush, Gupta, Nitin, Talwar, Tejinder, Gupta, Munish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489068/
https://www.ncbi.nlm.nih.gov/pubmed/26167228
http://dx.doi.org/10.4103/1817-1745.159205
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author Sharma, Ankush
Gupta, Nitin
Talwar, Tejinder
Gupta, Munish
author_facet Sharma, Ankush
Gupta, Nitin
Talwar, Tejinder
Gupta, Munish
author_sort Sharma, Ankush
collection PubMed
description Möbius syndrome is a rare congenital disorder presenting with facial diplegia and horizontal gaze disturbance. Patients can have additional cranial nerve palsies and musculoskeletal deformities. Neurofibromatosis Type 1 is an uncommon neurocutaneous disorder. The only plausible link between these two disorders is autosomal dominant pattern of inheritance. Simultaneous occurrence of these two uncommon disorders has not been yet reported in literature, and it is the first case report to the best of our knowledge.
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spelling pubmed-44890682015-07-12 Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence Sharma, Ankush Gupta, Nitin Talwar, Tejinder Gupta, Munish J Pediatr Neurosci Case Report Möbius syndrome is a rare congenital disorder presenting with facial diplegia and horizontal gaze disturbance. Patients can have additional cranial nerve palsies and musculoskeletal deformities. Neurofibromatosis Type 1 is an uncommon neurocutaneous disorder. The only plausible link between these two disorders is autosomal dominant pattern of inheritance. Simultaneous occurrence of these two uncommon disorders has not been yet reported in literature, and it is the first case report to the best of our knowledge. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4489068/ /pubmed/26167228 http://dx.doi.org/10.4103/1817-1745.159205 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sharma, Ankush
Gupta, Nitin
Talwar, Tejinder
Gupta, Munish
Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence
title Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence
title_full Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence
title_fullStr Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence
title_full_unstemmed Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence
title_short Möbius syndrome associated with neurofibromatosis Type 1: A rare co-occurrence
title_sort möbius syndrome associated with neurofibromatosis type 1: a rare co-occurrence
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489068/
https://www.ncbi.nlm.nih.gov/pubmed/26167228
http://dx.doi.org/10.4103/1817-1745.159205
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