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Results 1 - 10 of 86 for Mild hearing impairment
  1. Norrie disease 
    ... carrier females have shown some retinal abnormalities or mild hearing loss associated with Norrie disease. Females with one NDP ...
    https://medlineplus.gov/genetics/condition/norrie-disease - Genetics
  2. Wolfram syndrome 
    ... in severity from deafness beginning at birth to mild hearing loss beginning in adolescence that worsens over time. Sixty ...
    https://medlineplus.gov/genetics/condition/wolfram-syndrome - Genetics
  3. Renal coloboma syndrome 
    ... vesicoureteral reflux), multiple kidney cysts, loose joints, and mild hearing loss. The prevalence of renal coloboma syndrome is unknown; ...
    https://medlineplus.gov/genetics/condition/renal-coloboma-syndrome - Genetics
  4. Spastic paraplegia type 7 
    ... swallowing (dysphagia); involuntary movements of the eyes (nystagmus); mild hearing loss; abnormal curvature of the spine (scoliosis); high-arched ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  5. Deafness-dystonia-optic neuronopathy syndrome 
    ... gene are typically unaffected; however, they may develop mild hearing loss and dystonia. A characteristic of X-linked inheritance ...
    https://medlineplus.gov/...ness-dystonia-optic-neuronopathy-syndrome - Genetics
  6. GJB2 gene 
    ... recessive nonsyndromic hearing loss. It is characterized by mild to profound hearing loss that is present before a child learns to ... after a child learns to speak (postlingual). The hearing loss ranges from mild to profound, becomes more severe over time, and ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  7. Townes-Brocks Syndrome 
    ... of Townes-Brocks syndrome can include kidney abnormalities, mild to profound hearing loss, eye abnormalities, heart defects, foot abnormalities, and genital ...
    https://medlineplus.gov/genetics/condition/townes-brocks-syndrome - Genetics
  8. Alpha-N-acetylgalactosaminidase deficiency 
    ... typically diagnosed in adulthood. Affected individuals may have mild cognitive impairment and hearing loss caused by abnormalities of the inner ear ( ...
    https://medlineplus.gov/...lpha-n-acetylgalactosaminidase-deficiency - Genetics
  9. CHARGE syndrome 
    ... is diminished (hyposmia) or completely absent (anosmia), and mild to profound hearing loss. People with CHARGE syndrome also typically have middle ...
    https://medlineplus.gov/genetics/condition/charge-syndrome - Genetics
  10. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... with ADCADN have difficulty coordinating movements (ataxia) and mild to moderate hearing loss caused by abnormalities of the inner ear (sensorineural ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
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