Phenotypic characterization of DFNA24: prelingual progressive sensorineural hearing impairment

Audiol Neurootol. 2006;11(5):269-75. doi: 10.1159/000093525. Epub 2006 May 23.

Abstract

This article describes the hearing impairment (HI) phenotype which segregates in a large multi-generation Swiss-German family with autosomal dominant nonsyndromic HI. The locus segregating within this pedigree is located on chromosome 4q35-qter and is designated as DFNA24. For this pedigree, audiometric data on 25 hearing-impaired family members are available. It was demonstrated that within this kindred the HI is sensorineural, bilateral, prelingual in onset, and progressive throughout life. Age-related typical audiograms depict steeply down-sloping curves, with moderate high-frequency HI at birth, then steady progression to moderate HI in the low frequencies, severe HI at mid-frequencies and profound HI at high frequencies by age 70. Annual threshold deterioration was approximately 0.5 dB/year at 1-2 kHz after correction for presbycusis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Audiometry, Pure-Tone
  • Auditory Threshold
  • Child
  • Chromosomes, Human, Pair 4 / genetics*
  • Cross-Sectional Studies
  • Disease Progression
  • Female
  • Genes, Dominant / genetics*
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Linear Models
  • Male
  • Middle Aged
  • Pedigree
  • Phenotype
  • Syndrome