VERTIGO, BENIGN RECURRENT
General Information (adopted from Orphanet):
| Synonyms, Signs: |
VERTIGO, BENIGN PAROXYSMAL POSITIONAL BRV1, INCLUDED VERTIGO, BENIGN RECURRENT, 1, INCLUDED VESTIBULOPATHY, FAMILIAL BRV BPPV |
| Number of Symptoms | 8 |
| OrphanetNr: | |
| OMIM Id: |
193007
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| ICD-10: |
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| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant inheritance [Omim] |
| Age of onset: |
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Disease classification (adopted from Orphanet):
| Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0002321) | Vertigo | 58 / 7739 | ||||
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(HPO:0002141) | Gait imbalance | 55 / 7739 | ||||
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(OMIM) | Vestibulopathy, bilateral, progressive | 1 / 7739 | ||||
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(OMIM) | No hearing loss | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(MedDRA:10052087) | Oscillopsia | 3 / 7739 | ||||
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(OMIM) | Episodic vertigo | 4 / 7739 | ||||
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(HPO:0003677) | Slow progression | 134 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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Additional Information:
| Description: (OMIM) |
Benign recurrent vertigo (BRV), also known as benign paroxysmal positional vertigo (BPPV), is a common disorder affecting up to 2% of the adult population. The majority of individuals with chronic recurrent vertigo have no identifiable cause, no progression ... |
| Clinical Description OMIM |
Baloh et al. (1994) described 3 patients who presented with episodic vertigo followed by gait imbalance and oscillopsia and were found to have profound bilateral vestibular loss despite normal hearing. All had a parent with similar findings. The ... |