Otolaryngology and Communication Enhancement

Sensorineural hearing loss (SNHL) is usually permanent hearing loss that results when something is not working in the cochlea (or other parts of the inner ear), hearing nerve or brain. If you/your child have this type of hearing loss (with a newborn/childhood onset), you may qualify for one or more of the following studies:

Gene Chip Study - We have created a Deafness GeneChip that allows us to simultaneously screen for mutations in many different genes that are known to cause deafness. We are currently validating our GeneChip, to determine its performance characteristics. To do this we are recruiting individuals who have:

Connexin 26 Study - We are studying the relationship between Connexin 26 mutations and hearing loss, particularly variations in the characteristics of the hearing loss. If you or your child has hearing loss caused by Connexin 26 and/or Connexin 30 mutations, he/she can be a participant in this study.

Novel Gene Discovery Study - We are searching for novel genes involved in hearing loss by studying large families with inherited hearing loss. If you have a large family with hearing loss (five or more persons with hearing loss) and are interested in participating in a study to find the responsible gene, please contact us.

If you have any questions about the studies or if you are interested in becoming a participant, please contact our research assistant, Anna Frangulov at (617) 515-2962 or anna.frangulov@childrens.harvard.edu

If you are interested in learning more about the genetic causes of hearing loss, and/or interested in receiving free educational booklets, please visit Harvard Medical School Center of Hereditary Deafness.