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Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation

Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation: Introduction

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.

Symptoms of Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation

Home Diagnostic Testing

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Wrongly Diagnosed with Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation?

Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation: Complications

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Causes of Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation

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Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation

Heart attacks can be undiagnosed: Although the most severe symptoms of heart attack are hard to miss, there are varying degrees of severity. It...read more »

Heart attacks can be overdiagnosed: Although many people die from heart attacks, there are also many cases where people fear that they have a...read more »

Rare heart condition often undiagnosed: The rare heart condition called long QT syndrome can lead to episodes of palpitations and rapid heartbeat. In rare cases, this undiagnosed condition...read more »

Heart attack can be over-diagnosed: Although heart attack is often undiagnosed, leading to fatality, it can also be over-diagnosed. People become concerned that a condition is a heart attack,...read more »

Alzheimer's disease over-diagnosed: The well-known disease of Alzheimer's disease is often over-diagnosed. Patients tend to assume that any...read more »

Dementia may be a drug interaction: A common scenario in aged care is for a patient to show mental decline to dementia. Whereas this can, of course, occur due to various...read more »

Tremor need not be Parkinson's disease: There is the tendency to believe that any tremor symptom, or shakiness, means Parkinson's disease. The reality is that there are various possibilities, such as benign essential tremor, which...read more »

Blood pressure cuffs misdiagnose hypertension in children: One known misdiagnosis issue with hyperension, arises in relation to the simple equipment used to test blood...read more »

Rare diseases misdiagnosed as Parkinson's disease: A rare genetic disorder is often misdiagnosed as Parkinson's disease for men in their 50's....read more »

Hypertension misdiagnosis common in children: Hypertension is often misdiagnosed in adults (see misdiagnosis of hypertension), but its misdiagnosis is even more likely in children. Some of the symptoms of hypertension that can be...read more »

Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation: Research Doctors & Specialists

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Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation: Rare Types

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Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation: Animations

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More information about Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation

  1. Cardiomyopathy -- hearing loss, type t RNA lysine gene mutation: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Types
  8. Complications
 

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