Vestibular Diseases

"Vestibular Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Pathological processes of the VESTIBULAR LABYRINTH which contains part of the balancing apparatus. Patients with vestibular diseases show instability and are at risk of frequent falls.

Descriptor ID

D015837

MeSH Number(s)

C09.218.568.900

Concept/Terms

Vestibular Diseases

Below are MeSH descriptors whose meaning is more general than "Vestibular Diseases".

Diseases [C]
Otorhinolaryngologic Diseases [C09]
Ear Diseases [C09.218]
Labyrinth Diseases [C09.218.568]
Vestibular Diseases [C09.218.568.900]

Below are MeSH descriptors whose meaning is related to "Vestibular Diseases".

Below are MeSH descriptors whose meaning is more specific than "Vestibular Diseases".

Vestibular Diseases
Vertigo

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Vestibular Diseases" by people in Harvard Catalyst Profiles by year, and whether "Vestibular Diseases" was a major or minor topic of these publication.

Bar chart showing 129 publications over 30 distinct years, with a maximum of 9 publications in 2015 and 2022

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1994	1	0	1
1995	3	1	4
1996	0	2	2
1997	1	1	2
1998	2	0	2
1999	2	0	2
2000	2	0	2
2001	3	0	3
2002	2	0	2
2003	2	0	2
2004	4	1	5
2005	7	1	8
2006	4	1	5
2007	2	1	3
2008	4	2	6
2009	5	0	5
2010	5	1	6
2011	6	0	6
2012	2	1	3
2013	3	0	3
2014	6	0	6
2015	9	0	9
2016	4	2	6
2017	2	0	2
2018	5	2	7
2019	5	1	6
2020	2	1	3
2021	5	0	5
2022	7	2	9
2023	4	0	4

Below are the most recent publications written about "Vestibular Diseases" by people in Profiles.

Characterizing the molecular impact of KMT2D variants on the epigenetic and transcriptional landscapes in Kabuki syndrome. Hum Mol Genet. 2023 06 19; 32(13):2251-2261.

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Insights into the genotype-phenotype relationship of ocular manifestations in Kabuki syndrome. Am J Med Genet A. 2023 05; 191(5):1325-1338.

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Association of Ear Anomalies and Hearing Loss Among Children With 22q11.2 Deletion Syndrome. Otolaryngol Head Neck Surg. 2023 04; 168(4):856-861.

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Benign paroxysmal vertigo of childhood. Handb Clin Neurol. 2023; 198:229-240.

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Vergence and Accommodation Deficits in Children and Adolescents with Vestibular Disorders. Optom Vis Sci. 2022 12 01; 99(12):859-867.

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Truncating Variants in RFC1 in Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome. Neurology. 2023 01 31; 100(5):e543-e554.

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An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome. Am J Hum Genet. 2022 Oct 06; 109(10):1867-1884.

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Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency. Hum Mol Genet. 2022 09 10; 31(18):3083-3094.

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Evaluation and management of paediatric vertigo. Curr Opin Otolaryngol Head Neck Surg. 2022 Dec 01; 30(6):431-437.

View in: PubMed
Evidence for cognitive impairment in patients with vestibular disorders. J Neurol. 2022 Nov; 269(11):5831-5842.

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