Bilateral Sensorineural Hearing Loss Associated With the Point Mutation in Mitochondrial Genome
โ Scribed by Takeshi Oshima; Narihisa Ueda; Katsuhisa Ikeda; Koji Abe; Tomonori Takasaka
- Book ID
- 114497199
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 622 KB
- Volume
- 106
- Category
- Article
- ISSN
- 0023-852X
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
We report a French pedigree with members having an inherited combination of non-epidermolytic palmoplantar keratoderma (NEPPK) and sensorineural deafness. The penetrance of both features was incomplete. Additional ectodermal defects were absent. The expression of numerous epidermal proteins (keratin
## Abstract Several mitochondrial DNA variants increase risk for developing sensorineural hearing loss following exposure to aminoglycoside antibiotics, a particular concern in the premature infant population, as many of these babies spend time in neonatal intensive care units and are treated with