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Autosomal dominant nonsyndromic hearing loss 2A

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Description

DFNA2 nonsyndromic hearing loss is characterized by symmetric, predominantly high-frequency sensorineural hearing loss (SNHL) that is progressive across all frequencies. At younger ages, hearing loss tends to be mild in the low frequencies and moderate in the high frequencies; in older persons, the hearing loss is moderate in the low frequencies and severe to profound in the high frequencies. Although the hearing impairment is often detected during routine hearing assessment of a school-age child, it is likely that hearing is impaired from birth, especially at high frequencies. Most affected persons initially require hearing aids to assist with sound amplification between ages ten and 40 years. By age 70 years, all persons with DFNA2 nonsyndromic hearing loss have severe-to-profound hearing impairment.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

28

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Genes

External Links

  • OMIM

    600101

  • Orphanet
  • HPO
  • Medgen

    C2677637

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