Hearing loss and Turner syndrome


Contributed by Debbie Clason, staff writer, Healthy Hearing

Parents of girls who don’t appear to be developing at the same rate as their peers and who suffer from frequent ear infections may want to ask their family doctor if she should be tested for Turner syndrome, a rare genetic condition which affects one out of every 2,000 – 4,000 female births. Early diagnosis is key, as those affected have higher incidences of heart, liver and kidney abnormalities, autoimmune disorders, chronic ear infections and hearing loss.

About Turner syndrome

Turner syndrome
Turner syndrome is rare, but can have 

hearing health complications.

Among the 23 pairs of chromosomes in the human body are two sex chromosomes which differentiate men from women. Men have one X and one Y chromosome in their cells while females have two X chromosomes. When females are missing all or part of the second X chromosome, it can cause a condition known as Turner syndrome. The condition is named after Dr. Henry Turner, who first described the condition in 1938.

This chromosomal condition, which prevents the female body from growing and maturing naturally, can be diagnosed anytime during pregnancy, infancy, late pre-teen or early adolescence. Although each individual is unique, physical characteristics may include short stature, down-turning eyelids, low set and prominent ears, and a small jaw. A blood test is typically used to diagnose the syndrome.

How Turner syndrome affects hearing

According to a study published in the Brazilian Journal of Otolaryngology, those with Turner syndrome have a high prevalence of problems with their hearing and should be evaluated frequently. Common problems include chronic ear infections as well as conductive and sensorineural hearing loss.

  • Chronic infections of the middle ear affect as much as 88 percent of this population, according to the Brazilian study. Researchers said this percentage decreases with age and is almost absent by adolescent. 
  • Cholesteatoma can be more prevalent among girls with Turner syndrome due to frequent ear infections. While these cyst-like growths are not malignant, they can cause further hearing complications, trouble with balance and dizziness and even meningitis if left untreated. 
  • Conductive hearing loss among those with Turner syndrome is estimated to be as high as 80 percent, mainly due to problems with the Eustachian tube and the high incidence of chronic ear infections. Although the condition is not progressive, it can interfere with speech and language development when left untreated.
  • Sensorineural hearing loss (SNHL) appears in late childhood/early adulthood and affects as many as 90 percent of this population. SNHL is progressive, meaning the hearing loss generally worsens with age. Most cases of SNHL can be treated with hearing devices such as hearing aids or cochlear implants, depending upon the severity of the hearing loss.

Talk to your doctor

If you suspect a female member of your family has Turner syndrome, talk to your family physician. They may refer you to a pediatric endocrinologist for further testing. Additional information and resources about this condition are available at The Turner Syndrome Society of the United States. The organization also has a robust Facebook community where families can post questions, share personal stories and get support.

Even though the chances that your relative has Turner syndrome are low, it’s always a good idea to begin monitoring hearing health at an early age. It all begins with establishing a good rapport with a hearing healthcare professional. To find one you can trust with your family’s hearing health, visit our directory of hearing centers.


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