Diseases Studied
The Rare Diseases Clinical Research Network is an NIH-funded research network of 20 active consortia or research groups working to advance treatment for diseases that are rare. Use the search tools on this page to find the diseases we currently study. You can reach out to the indicated consortia or research groups for more information on those diseases and studies underway.
This network focuses on clinical research and does not generally support clinical care outside of research activities. To learn about other rare diseases, please visit the Genetic and Rare Diseases Information Center (GARD), which is an NIH program that helps the public find reliable information about rare and genetic diseases. Their staff are specialists. Contact them at 1-888-205-2311 or email GARDinfo@nih.gov.
All Diseases > Aminoglycoside-induced deafness
Aminoglycoside-induced deafness (AID)
Disease Category: Mitochondrial Disorders
Sensorineural hearing loss, or permanent hearing loss caused by irreversible damage to the inner ear or the nerve that transmits signals from the brain to the ear. Onset occurs a few days to weeks following exposure to aminoglycoside antibiotics. Specific genetic mutations in mitochondria (specialized cellular structures that produce energy) predispose individuals to ototoxicity (ear poisoning by certain medications).
Research groups studying this disease
Mitochondrial Disorders
North American Mitochondrial Disease Consortium (NAMDC)
United Mitochondrial Disease Foundation
Promotes research and education for the diagnosis, treatment, and cure of mitochondrial disorders while providing support to those affected.
MitoAction
Improves quality of life for people affected by mitochondrial disease through education, outreach, advocacy, and clinical research initiatives.