Literature DB >> 16229900

Congenital unilateral multiple cranial neuropathy: an etiology shared with Mobius syndrome?

Brian M Allen1, Matthew A Wert, Sherard A Tatum.   

Abstract

Mobius syndrome was originally described as bilateral 6th and 7th cranial nerve palsy and has since been expanded to include involvement of nearly all cranial nerves, limb deformities, orofacial anomalies and deficits in intellectual function. The etiology of Mobius syndrome remains elusive. Here we present a case with unilateral 5th, 7th, 9th, 10th and 12th cranial nerve palsy along with MRI evidence of ipsilateral brainstem hypoplasia. We propose the unilateral pathology supports the theory that vascular malformation in utero, which can be due to various etiologies, leads to brainstem ischemia and is the key factor in development of Mobius syndrome.

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Year:  2005        PMID: 16229900     DOI: 10.1016/j.ijporl.2005.09.013

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  3 in total

1.  Moebius syndrome: Craniofacial clinical manifestations and their association with prenatal exposure to misoprostol.

Authors:  Néstor O Ruge-Peña; Claudia Valencia; Dagoberto Cabrera; Daniel C Aguirre; Francisco Lopera
Journal:  Laryngoscope Investig Otolaryngol       Date:  2020-08-03

Review 2.  Imaging the cranial nerves: Part I: methodology, infectious and inflammatory, traumatic and congenital lesions.

Authors:  Alexandra Borges; Jan Casselman
Journal:  Eur Radiol       Date:  2007-02-24       Impact factor: 7.034

3.  Möbius syndrome: misoprostol use and speech and language characteristics.

Authors:  Zelita Caldeira Ferreira Guedes
Journal:  Int Arch Otorhinolaryngol       Date:  2014-03-21
  3 in total

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