Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 68 for ear disorders
  1. ... hearing loss caused by abnormalities of the inner ear (sensorineural deafness), and excessive daytime sleepiness (narcolepsy). Cognitive decline occurs as the disorder progresses. Numbness, tingling, or pain in the arms ...
  2. ... been found to cause auriculo-condylar syndrome, a disorder that primarily affects the development of the ears and lower jaw (mandible). The identified mutations change ...
  3. ... is also found in the kidneys and inner ear. A combination of CLCNKA and CLCNKB gene mutations causes a life-threatening form of the disorder known as Bartter syndrome type IV or antenatal ...
  4. ... proper pH of the fluid in the inner ear (endolymph). Several ATP6V0A4 gene mutations have been identified in people with renal tubular acidosis with deafness, a disorder involving excess acid in the blood (metabolic acidosis), ...
  5. ... is also found in the kidneys and inner ear. A combination of CLCNKA and CLCNKB gene mutations causes a life-threatening form of the disorder called Bartter syndrome type IV. This condition is ...
  6. ... been found to cause auriculo-condylar syndrome, a disorder that primarily affects the development of the ears and lower jaw (mandible). The identified mutations change ...
  7. ... vessels in the retina and in the inner ear. Several NDP gene variants (also called mutations) have been found to cause the eye disorder familial exudative vitreoretinopathy. This disorder affects the retina ...
  8. ... can have chronic respiratory and sinus infections, recurrent ear infections (otitis media), and hearing loss.It is unclear why mutations in the RPGR gene can cause a variety of disorders. Studies suggest that certain mutations may disrupt the ...
  9. ... proper pH of the fluid in the inner ear (endolymph). More than 25 ATP6V1B1 gene mutations have been identified in people with renal tubular acidosis with deafness, a disorder involving excess acid in the blood (metabolic acidosis), ...
  10. ... in the development of the brain, eyes, inner ear, heart, and kidneys. More than 15 mutations in the RERE gene have been found to cause a condition called neurodevelopmental disorder with or without anomalies of the brain, eye, ...
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next