Literature DB >> 25814660

Cranial Nerve Abnormalities in Oculo-Auriculo-Vertebral Spectrum.

R Manara1, D Brotto2, S Ghiselli2, R Mardari3, I Toldo4, G Schifano2, E Cantone5, R Bovo2, A Martini2.   

Abstract

BACKGROUND AND
PURPOSE: Cranial nerve abnormalities might be observed in hemifacial microsomia and microtia (oculo-auriculo-vertebral spectrum), but the rate, features, and relationship with functional impairment or phenotype severity have not yet been defined. This study aimed at investigating absence/asymmetry, abnormal origin, morphology and course of cranial nerves, and presence/asymmetry of the foramen ovale and inferior alveolar nerve canal in a cohort of oculo-auriculo-vertebral spectrum patients.
MATERIALS AND METHODS: Twenty-nine patients with oculo-auriculo-vertebral spectrum (mean age, 7 years; age range, 0.2-31 years; 12 females) underwent brain MR imaging, CT, and neurologic evaluation; 19 patients had a more severe phenotype (Goldenhar syndrome).
RESULTS: Cranial nerve abnormalities were detected only in patients with Goldenhar syndrome (17/19, bilaterally in 8) and were involved the second (4/19), third (1/18), fifth (11/19), sixth (8/16), seventh (11/18), and eighth (8/18) cranial nerves. Multiple cranial nerve abnormalities were common (11/17). Eleven patients showed bone foramina abnormalities. Trigeminal and facial nerve dysfunctions were common (44% and 58%, respectively), especially in patients with Goldenhar syndrome. Trigeminal abnormalities showed a good correlation with ipsilateral dysfunction (P = .018), which further increased when bone foramina abnormalities were included. The facial nerve showed a trend toward correlation with ipsilateral dysfunction (P = .081). Diplopia was found only in patients with Goldenhar syndrome and was associated with third and sixth cranial nerve abnormalities (P = .006).
CONCLUSIONS: Among patients with oculo-auriculo-vertebral spectrum, cranial nerve morphologic abnormalities are common, correlate with phenotype severity, and often entail a functional impairment. The spectrum of cranial nerve abnormalities appears wider than simple hypo-/aplasia and includes an anomalous cisternal course and partial/complete fusion of diverse cranial nerves.
© 2015 by American Journal of Neuroradiology.

Entities:  

Mesh:

Year:  2015        PMID: 25814660      PMCID: PMC7965278          DOI: 10.3174/ajnr.A4273

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  30 in total

1.  The cochlear nerve canal and internal auditory canal in children with normal cochlea but cochlear nerve deficiency.

Authors:  Fei Yan; Jianhong Li; Junfang Xian; Zhenchang Wang; Lingyan Mo
Journal:  Acta Radiol       Date:  2013-01-14       Impact factor: 1.990

2.  Ocular aspects of Goldenhar's syndrome.

Authors:  J L Baum; M Feingold
Journal:  Am J Ophthalmol       Date:  1973-02       Impact factor: 5.258

3.  Oculoauricular vertebral dysplasia. Its association with sensorineural deafness and other abnormalities.

Authors:  S S Budden; G C Robinson
Journal:  Am J Dis Child       Date:  1973-03

4.  The oculoauriculovertebral dysplasia syndrome of Goldenhar.

Authors:  H S Sugar
Journal:  Am J Ophthalmol       Date:  1966-10       Impact factor: 5.258

Review 5.  The first and second branchial arch syndrome.

Authors:  W C Grabb
Journal:  Plast Reconstr Surg       Date:  1965-11       Impact factor: 4.730

6.  Apparent cochlear nerve aplasia: to implant or not to implant?

Authors:  Frank M Warren; Richard H Wiggins; Cache Pitt; H Ric Harnsberger; Clough Shelton
Journal:  Otol Neurotol       Date:  2010-09       Impact factor: 2.311

7.  Ocular findings in the facioauriculovertebral sequence (Goldenhar-Gorlin syndrome).

Authors:  A M Mansour; F Wang; P Henkind; R Goldberg; R Shprintzen
Journal:  Am J Ophthalmol       Date:  1985-10-15       Impact factor: 5.258

8.  Radiologic evidence for absence of the facial nerve in Möbius syndrome.

Authors:  Harriëtte T F M Verzijl; Jaap Valk; Rob de Vries; George W Padberg
Journal:  Neurology       Date:  2005-03-08       Impact factor: 9.910

9.  Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomaly.

Authors:  Sirpa Ala-Mello; Linda Siggberg; Sakari Knuutila; Harriet von Koskull; Mervi Taskinen; Maarit Peippo
Journal:  Am J Med Genet A       Date:  2008-10-01       Impact factor: 2.802

10.  Cochlear implantation in children with cochlear nerve deficiency.

Authors:  Vincenzo Vincenti; Francesca Ormitti; Elisa Ventura; Maurizio Guida; Alessia Piccinini; Enrico Pasanisi
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2014-03-12       Impact factor: 1.675

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  5 in total

1.  Salivary glands abnormalities in oculo-auriculo-vertebral spectrum.

Authors:  Davide Brotto; Renzo Manara; Stefania Vio; Sara Ghiselli; Elena Cantone; Rodica Mardari; Irene Toldo; Valentina Stritoni; Alessandro Castiglione; Elisa Lovo; Patrizia Trevisi; Roberto Bovo; Alessandro Martini
Journal:  Clin Oral Investig       Date:  2017-05-22       Impact factor: 3.573

2.  Oculo-auriculo-vertebral spectrum: going beyond the first and second pharyngeal arch involvement.

Authors:  Brotto Davide; Manara Renzo; Ghiselli Sara; Lovo Elisa; Mardari Rodica; Toldo Irene; Castiglione Alessandro; Schifano Giovanni; Stritoni Valentina; Bovo Roberto; Trevisi Patrizia; Martini Alessandro
Journal:  Neuroradiology       Date:  2017-03-01       Impact factor: 2.804

3.  A new lumbar vertebral anomaly in Goldenhar syndrome: A case report.

Authors:  Mauro Costa Morais Tavares Junior; Dennis J Heaton; Brian M Everist; Brandon B Carlson
Journal:  Radiol Case Rep       Date:  2022-04-17

4.  Behavioral Adjustment of Preschool Children With and Without Craniofacial Microsomia.

Authors:  Alexis L Johns; Erin R Wallace; Brent R Collett; Kathleen A Kapp-Simon; Amelia F Drake; Carrie L Heike; Sara L Kinter; Daniela V Luquetti; Leanne Magee; Susan Norton; Kathleen Sie; Matthew L Speltz
Journal:  Cleft Palate Craniofac J       Date:  2020-08-12

5.  Bezold's abscess secondary to os tympanicum cholesteatoma in Goldenhar syndrome.

Authors:  Matteo Minerva; Silvia Valeggia; Stefano Fusetti; Elisabetta Zanoletti; Renzo Manara; Davide Brotto
Journal:  BJR Case Rep       Date:  2021-03-26
  5 in total

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