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72 Possible Causes for Severe to Profound Congenital Sensorineural Hearing Loss

  • Congenital Deafness

    Usher syndrome type I is characterized by congenital severe-to-profound sensorineural hearing loss and vestibular dysfunction.[nature.com] sensorineural hearing loss.[dizziness-and-balance.com] Autosomal recessive syndromic hearing impairment Pendred syndrome Pendred syndrome is the most common form of syndromic hearing loss and is characterized by congenital severe-to-profound[nature.com]

  • Deafness

    Mumps (Epidemic parotitis) may result in profound sensorineural hearing loss (90 dB or more), unilateral (one ear) or bilateral (both ears). congenital rubella (also called[en.wikipedia.org] Measles may cause auditory nerve damage but usually gives rise to a chronic middle ear problem giving rise to a mixed hearing loss.[en.wikipedia.org] German measles) syndrome, can cause deafness in newborns several varieties of herpes viruses that cause other diseases can also infect the ear, and can result in hearing[en.wikipedia.org]

  • High Myopia-Sensorineural Deafness Syndrome

    Recessive Usher Syndrome Congenital sensorineural hearing loss Type 1 Severe to profound hearing loss Abnormal vestibular function Delayed walking and sitting Type 2 mild[en.wikibooks.org] It is characterized by congenital severe-to-profound sensorineural hearing impairment and euthyroid goiter. Goiter develops in early puberty or adulthood.[emedicine.medscape.com] Usher syndrome type I is characterized by congenital severe-to-profound sensorineural hearing loss and vestibular dysfunction.[nature.com]

  • Autosomal Dominant Deafness 9

    Recessive Usher Syndrome Congenital sensorineural hearing loss Type 1 Severe to profound hearing loss Abnormal vestibular function Delayed walking and sitting Type 2 mild[en.wikibooks.org] Hearing loss can be classified based on age at onset (pre or post-lingual), type of ear defect (conductive, sensorineural or mixed), degree of hearing loss (mild, moderate[mafiadoc.com] Usher syndrome type I is characterized by congenital severe-to-profound sensorineural hearing loss and vestibular dysfunction.[nature.com]

  • Sensorineural Hearing Impairment

    It is characterized by congenital severe-to-profound sensorineural hearing impairment and euthyroid goiter. Goiter develops in early puberty or adulthood.[emedicine.medscape.com] loss.[emedicine.medscape.com] […] compound heterozygous mutations) in two Chinese families affected by Usher syndrome. [21] Pendred syndrome Pendred syndrome is the second most common type of AR syndromic hearing[emedicine.medscape.com]

  • Autosomal Dominant Deafness 11

    Recessive Usher Syndrome Congenital sensorineural hearing loss Type 1 Severe to profound hearing loss Abnormal vestibular function Delayed walking and sitting Type 2 mild[en.wikibooks.org] Usher type 2A Autosomal recessive USH2A Extracellular matrix protein Congenital moderate-to-severe sensorineural hearing loss (normal vestibular function) and retinitis pigmentosa[academic.oup.com] sensorineural hearing loss.[dizziness-and-balance.com]

  • Autosomal Recessive Deafness 22

    Recessive Usher Syndrome Congenital sensorineural hearing loss Type 1 Severe to profound hearing loss Abnormal vestibular function Delayed walking and sitting Type 2 mild[en.wikibooks.org] sensorineural hearing loss.[dizziness-and-balance.com] […] aids Cochlear implants Educational intervention Common causes of Genetic hearing loss [ edit ] Syndromic Hearing loss [ edit ] (Accounts for 30% prelingual deafness) Autosomal[en.wikibooks.org]

  • Autosomal Recessive Deafness 76

    Prevalence of GBJ2 mutations in patients with severe to profound congenital non-syndromic sensorineural hearing loss in Bulgarian population.[degruyter.com] Usher type 2A Autosomal recessive USH2A Extracellular matrix protein Congenital moderate-to-severe sensorineural hearing loss (normal vestibular function) and retinitis pigmentosa[academic.oup.com] Usher type 1E Autosomal recessive PCD15 Protocadherin Profound congenital deafness, retinitis pigmentosa, vestibular arreflexia.[academic.oup.com]

  • Autosomal Recessive Deafness 42

    Affected members in these families were described with congenital or prelingual, severe-to-profound sensorineural hearing loss (Table 2 ).[karger.com] sensorineural hearing loss.[dizziness-and-balance.com] loss [Chen et al., 2005; Miyagawa et al., 2013; Chakchouk et al., 2015; Sloan-Heggen et al., 2015].[karger.com]

  • Autosomal Dominant Deafness 64

    Usher syndrome type I is characterized by congenital severe-to-profound sensorineural hearing loss and abnormal vestibular dysfunction.[consilieregenetica.org] Usher type 2A Autosomal recessive USH2A Extracellular matrix protein Congenital moderate-to-severe sensorineural hearing loss (normal vestibular function) and retinitis pigmentosa[academic.oup.com] The syndrome is characterized by congenital sensorineural hearing loss that is usually (though not invariably) severe-to-profound and euthyroid goiter.[consilieregenetica.org]

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