Hearing Health Newsletter: July 2026

Image: A 3D reconstruction of a bony channel called the vestibular aqueduct (VA) on the left, compared with one that is abnormally shaped on the right. Credit: Robles-Bolivar et al./JAMA Otolaryngology–Head & Neck Surgery

What if a rare bone disorder could help explain why some people develop Ménière’s disease? A new study from Emerging Research Grants (ERG) scientist Divya A. Chari, M.D., and team suggests that variants of a single gene may alter inner ear development decades before symptoms of fluctuating balance and hearing loss begin. Future imaging and genetic testing may help identify individuals at increased risk. (Recent research by Penn Medicine also links developmental genetics to adult vestibular conditions.)

Chari’s 2024 ERG grant was generously funded by an anonymous donor and renewed for a second year in 2025, generously funded by Karen I. Coley. The paper’s coauthors include HHF board member and 1999 ERG scientist Sharon G. Kujawa, Ph.D.

Plus: 


Planned Giving Matching Challenge

Your legacy gift supports the top-tier scientists in Hearing Health Foundation’s research programs, the Hearing Restoration Project and Emerging Research Grants. Right now your planned gift to HHF—such as a bequest or beneficiary designation of a retirement fund or life insurance policy—will be matched with our $1 million match challenge.


Around the Web:

Products and services are not endorsed by Hearing Health Foundation. Links provided are for informational purposes only, may require registration or subscription, and may expire.


Get this monthly newsletter in your inbox:  SIGN UP

Print Friendly and PDF