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Results 1 - 7 of 7 for "Low-frequency" hearing loss
  1. WFS1 gene 
    ... Shelton C, Lalwani AK. Two families with nonsyndromic low-frequency hearing loss harbor novel mutations in Wolfram syndrome gene 1. ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  2. Labyrinthitis and Vestibular Neuritis (Vestibular Disorders Association)  
    Dizziness and Vertigo/Specifics ... Dizziness and Vertigo ... Ear Infections/Specifics ... Ear Infections ... Vestibular Disorders Association ... Vestibular neuritis and labyrinthitis ...
    https://vestibular.org/.../labyrinthitis-and-vestibular-neuritis - External Health Links
  3. Hearing: Noise-Induced Hearing Loss (American Academy of Family Physicians)  
    Noise/Start Here ... Noise ... American Academy of Family Physicians
    https://familydoctor.org/.../noise-induced-hearing-loss/?adfree=true - External Health Links
  4. Hearing Aids: How to Choose the Right One (Mayo Foundation for Medical Education and Research)  
    Hearing Aids/Related Issues ... Hearing Aids ... Mayo Foundation for Medical Education and Research
    https://www.mayoclinic.org/.../hearing-aids/ART-20044116?p=1 - External Health Links
  5. Meniere disease 
    ... anywhere from 20 minutes to 24 hours. Hearing loss is often only in one ear, but it may affect both ears. Hearing tends to improve between attacks, but gets worse over time. Low frequency hearing is lost first. You also may have ...
    https://medlineplus.gov/ency/article/000702.htm - Medical Encyclopedia
  6. Burn-McKeown syndrome 
    ... abnormalities of the nasal passages, characteristic facial features, hearing loss, heart abnormalities, and short stature.In people with ... Some people with Burn-McKeown syndrome have congenital hearing loss in both ears which varies in severity among ...
    https://medlineplus.gov/genetics/condition/burn-mckeown-syndrome - Genetics
  7. TXNL4A gene 
    ... abnormalities of the nasal passages, characteristic facial features, hearing loss, heart abnormalities, and short stature. Most people with ... J, Ludecke HJ, Strom TM. Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations ...
    https://medlineplus.gov/genetics/gene/txnl4a - Genetics