[Phenotypic characterization of a DFNA6 family with low-frequency hearing loss]

HNO. 2004 Feb;52(2):132-6. doi: 10.1007/s00106-003-0912-0.
[Article in German]

Abstract

Background: Hereditary hearing impairment is a heterogeneous sensory defect with approximately two-thirds of all cases being nonsyndromic. Only two loci (DFNA1 and DFNA6/14/38) are associated with low frequency sensorineural nonsyndromic hearing impairment. DFNA6 was mapped to chromosome 4p16. Recessive mutations in the WFS1 gene are responsible for Wolfram syndrome; missense mutations inherited as an autosomal dominant result in low frequency sensorineural hearing impairment (LFSNHI).

Patients and methods: In this study we analyzed the phenotype of a large Hungarian family with LFSNHI and linkage to DFNA6. The family contains 14 affected persons.

Results and conclusion: In general, these patients show a postlingual, sensorineural, bilateral, symmetric, nonsyndromic low frequency hearing impairment with a slow progression. This impairment is accompanied by normal vision and normal vestibular responses.

Publication types

  • English Abstract

MeSH terms

  • Adolescent
  • Adult
  • Audiometry, Pure-Tone
  • Child
  • Chromosome Aberrations*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 4*
  • DNA Mutational Analysis
  • Disease Progression
  • Female
  • Genes, Dominant / genetics*
  • Genes, Recessive / genetics
  • Hearing Loss, Sensorineural / diagnosis
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Lod Score
  • Male
  • Membrane Proteins / genetics*
  • Mutation, Missense
  • Pedigree
  • Phenotype*
  • Pitch Perception*
  • Vestibular Function Tests
  • Wolfram Syndrome / diagnosis
  • Wolfram Syndrome / genetics*

Substances

  • Membrane Proteins
  • wolframin protein