Hearing loss in adult women with Turner's syndrome and other congenital hypogonadisms

Gynecol Endocrinol. 2014 Feb;30(2):111-6. doi: 10.3109/09513590.2013.856002. Epub 2013 Nov 20.

Abstract

Objectives: To define the patterns and causes of hearing decline associated to Turner's syndrome (TS).

Methods: An observational study with three cohorts was designed: 31 TS patients, 15 women with other congenital hypogonadims (OCH) and 41 healthy age-matched women taking contraception. Microotoscopy, standard pure-tone audiometry brain auditory evoked potentials (BAEP) were performed to study hearing function.

Results: Up to 87% of TS subjects suffered from some degree of hearing loss (HL) in the audiograms, compared with 20% OCH and 27% controls. Sensorineural hearing loss (SNHL) was the most frequent type of hypoacusia found in TS group. BAEP study demonstrated that 61% of TS women showed HL compared to 20% in OCH patients. No significant differences in latencies, amplitudes, and interpeaks of waves I, III and V were found between TS and OCH, nor when compared to reference population. Worse results were observed among the oldest TS patients, those with pure monosomy or isochromosome, and those with a history of recurrent otitis.

Conclusions: More than a half of TS females presented HL. SNHL is the most frequent pattern among middle-aged women with TS. Old age, karyotype and recurrent otitis are predisposition factors to produce HL, while oestrogens play a minor role.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Audiometry, Pure-Tone
  • Female
  • Hearing Loss / complications*
  • Hearing Loss / physiopathology
  • Humans
  • Hypogonadism / complications*
  • Hypogonadism / congenital
  • Hypogonadism / physiopathology
  • Middle Aged
  • Turner Syndrome / complications*
  • Turner Syndrome / physiopathology