Results 1 - 10 of 35 for Primary familial hypertrophic cardiomyopathy
  1. ... dilated cardiomyopathy? congestive cardiomyopathy familial idiopathic cardiomyopathy FDC primary familial dilated cardiomyopathy For more information about naming genetic conditions, see ...
  2. ... useful. Genetics and Health Resources for Patients and Families Resources for Health ... cell ; coma ; deficiency ; encephalopathy ; fasting ; fatty acids ; ...
  3. Genetics Home Reference: Cardiomyopathy From the National Institutes of Health (National Library of Medicine)  
    ... dilated cardiomyopathy familial dilated cardiomyopathy familial hypertrophic ... carnitine deficiency Salih myopathy You may also search ...
  4. What's Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    ... cardiomyopathy can then be broken down into: 1) "primary cardiomyopathy" where the heart is predominately affected and the ... under the age of 18 is diagnosed with primary cardiomyopathy. This annual incidence rate, however, is extremely conservative. ...
  5. Causes of Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    ... susceptible to contracting myocarditis. Isolated Familial Cases Isolated familial cardiomyopathy is considered when the child does not show ... or muscular disorders, and there is a known family history of cardiomyopathy. In affected families with HCM, ARVD, DCM, and ...
  6. ... common form. Some experts use the term "dilated cardiomyopathy" for cases where the primary problem is with the muscle itself. This definition ...
  7. Duchenne and Becker Muscular Dystrophies (Muscular Dystrophy Association) - PDF  
    ... DMD and BMD carriers are at risk for cardiomyopathy (see page 7). How can a family with no history of DMD or BMD suddenly ...
  8. Friedreich's Ataxia From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... diseases may also help affected individuals and their families cope with the disease. A primary care physician can screen people for complications such ...
  9. Familial Amyloidosis (Amyloidosis Foundation)  
    ... the first case in their family. Within each family disease begins at nearly the same age and symptoms usually include neuropathy and/or cardiomyopathy. Peripheral neuropathy begins as a lower extremity sensory ...
  10. ... useful. Genetics and Health Resources for Patients and Families Resources for Health ... decreased muscle tone ; deficiency ; dehydrogenase ; disability ; enzyme ; ...
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