IllnessMorbus Menière, familial; differential diagnosis
Summary
Short information
A curated panel containing 4 or 6 genes, respectively, for the comprehensive analysis of the suspected Morbus Menière, familial
ID
MP0170
Number of genes
5
Accredited laboratory test
Examined sequence length
5,3 kb (Core-/Core-canditate-Genes)
5,9 kb (Extended panel: incl. additional genes)
5,9 kb (Extended panel: incl. additional genes)
Analysis Duration
on request
Material
- EDTA-anticoagulated blood (3-5 ml)
Diagnostic indications
NGS +
Gene panel
Informations about the disease
Clinical Comment
Chronic illness characterized by intermittent episodes of vertigo lasting from min-h, with fluctuating sensorineural hearing loss, tinnitus + aural pressure
Synonyms
- Symptoms: Vertigo episodes, fluctuating sensorineural hearing loss, tinnitus, aural pressure
- Alias: Auditory vertigo
- Alias: Aural vertigo
- Alias: Otogenic vertigo
- Alias: Primary endolymphatic hydrops
- Allelic: Left ventricular noncompaction 1, with/-out congenital heart defects (DTNA)
- Deafness, AD 9 (COCH)
- Deafness, AR 110 (COCH)
- Menière "watchlist" [panelapp] (DPT)
- Susceptibility to Meniere disease (FAM136A)
- Susceptibility to Meniere disease (PRKCB1)
Heredity, heredity patterns etc.
- AD
OMIM-Ps
- Multiple OMIM-Ps
ICD10 Code
H91.8
Bioinformatics and clinical interpretation
No text defined