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. More detailed information about the symptoms, causes, and treatments of Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation is available below.
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