Literature DB >> 30635960

Vestibular dysfunction is a manifestation of 22q11.2 deletion syndrome.

Annelore Willaert1,2, Charlotte Van Eynde1, Nicolas Verhaert1,2, Christian Desloovere1, Vincent Vander Poorten1, Koenraad Devriendt3, Ann Swillen3, Greet Hens1.   

Abstract

The 22q11.2 deletion syndrome (22q11.2DS) is the second most common cause of developmental delay after Down syndrome. Impaired cognitive development is highly prevalent, but also motor abnormalities such as hypotonia and delays in achieving motor milestones are described. Instability is frequently detected in children, adolescents, and adults and is mostly attributed to their limited motor performance. Until now, vestibular function has not been investigated in these patients, despite the growing evidence that they often have inner ear malformations. The aim of this prospective study was to identify the presence and character of vestibular dysfunction in 22q11.2DS. We investigated 23 subjects with proven 22q11.2DS, older than the age of 12. We performed caloric testing and pendular rotation chair tests with videonystagmography, cervical vestibular-evoked myogenic potential (c-VEMP)-testing, and posturography. Additional otoscopy and audiometry were performed on all subjects. We found a unilateral caloric hypofunction in 55% of patients, a certain absent c-VEMP response in 15% of ears, an inconclusive c-VEMP response in 33% of ears, and abnormal posturography in 68% of patients, of whom 42% displayed a typical vestibular pattern. Remarkably, 90% revealed uni- or bilateral weak caloric responses, independent of caloric symmetry. Vestibular dysfunction is frequent in subjects with 22q11.2DS. This knowledge should be taken into account when assessing motor performance in these patients. Additional larger studies are needed to determine whether this dysfunction implicates a therapeutic potential.
© 2019 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals, Inc.

Entities:  

Keywords:  22q11 deletion syndrome; balance disorder; inner ear; labyrinth; motor development; velocardiofacial syndrome

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Year:  2019        PMID: 30635960     DOI: 10.1002/ajmg.a.7

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Case Report: Ménière's Disease-Like Symptoms in 22q11.2 Deletion Syndrome.

Authors:  Kwang-Dong Choi; Jeong-Yeon Kim; Seo-Young Choi; Eun Hye Oh; Hyun-Min Lee; Jieun Roh; Jae-Hwan Choi
Journal:  Front Neurol       Date:  2021-06-18       Impact factor: 4.003

2.  Vestibular Function Correlates with Radiologic Findings in a Gymnast with 22q11.2DS.

Authors:  Lindy M R Moxham; Arthur I Mallinson
Journal:  Am J Case Rep       Date:  2020-04-13
  2 in total

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