Cardiomyopathy hearing loss type t RNA lysine gene mutation


Cardiomyopathy - hearing loss, type t RNA lysine gene mutation: A rare inherited disorder characterized by heart muscle disease and deafness. The deafness is inherited from the mother and is caused by a genetic defect. Patients may be asymptomatic for a number of years. The rate of progression of the disorder is variable with some patients being asymptomatic until adulthood.


The list of signs and symptoms mentioned in various sources for Cardiomyopathy - hearing loss, type t RNA lysine gene mutation includes the 9 symptoms listed below:

  • Heart failure
  • Abnormal heart rhythm
  • Loss of cognitive skills
  • Progressive hearing loss
  • Slurred speech
  • Walking difficulties
  • Leg pain
  • Feeling of leg heaviness
  • Shortness of breath after exercising


  • Abnormal heart rhythm - see all causes of Abnormal heart rhythm
  • Heart failure - see all causes of Heart failure
  • Leg pain - see all causes of Leg pain
  • Progressive hearing loss - see all causes of Hearing impairment
  • Slurred speech - see all causes of Slurred speech
  • Walking difficulties - see all


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Heart Health: Home Testing:

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Ear Infections: Home Testing:

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  • Home Hearing Testing