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Results 1 - 10 of 29 for Familial hypertrophic cardiomyopathy 11
  1. ... type 8 Genetic Testing Registry: Arrhythmogenic right ventricular cardiomyopathy, type 9 Genetic Testing Registry: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILD PALMOPLANTAR KERATODERMA AND WOOLLY HAIR St. ...
  2. ... National Heart, Lung, and Blood Institute: What Is Cardiomyopathy? Educational resources - Information pages (11 links) Patient support - For patients and families (8 links) You may also be interested in ...
  3. Genetics Home Reference: Glutaric acidemia type II From the National Institutes of Health (National Library of Medicine)  
    ... useful. Genetics and health Resources for Patients and Families Resources for Health Professionals What ... (11 links) The resources on this site should not ...
  4. Duchenne and Becker Muscular Dystrophies (Muscular Dystrophy Association) - PDF  
    ... that may arise. Does It Run in the Family? 11 DMD/BMD • ©2011 MDA T he MDA website ...
  5. ... pages (14 links) Patient support - For patients and families (11 links) You may also be interested in these ... useful. Genetics and health Resources for Patients and Families Resources for Health ... chromosome ; dilated ; gene ; His ; inheritance ; inherited ; ...
  6. Diagnosis and Management of Duchenne Muscular Dystrophy: A Guide for Families (Parent Project for Muscular Dystrophy Research) - PDF  
    ... of the risk of heart rhythm problems and cardiomyopathy is important. Anesthetic risks (see Section 11) need to be taken into account at all ...
  7. JAMA Patient Page: Hypertrophic Cardiomyopathy (American Medical Association) - PDF  
    ... to a mutation in at least 1 of 11 genes coding for sarcomere protein. In persons without a family history of HCM, the most common cause is ...
  8. Genetics Home Reference: Schindler disease From the National Institutes of Health (National Library of Medicine)  
    ... useful. Genetics and health Resources for Patients and Families Resources for Health ... developmental delay ; enzyme ; gene ; glycolipids ; glycoproteins ; ...
  9. Mitochondrial Myopathies (Muscular Dystrophy Association) - PDF  
    ... or unknown mutations but may require samples from family members; this is more expensive and time-consuming. Diagnostic Tests in Mitochondrial Diseases 11 Mitochondrial Myopathies • ©2011 MDA This diagram depicts common ...
  10. ... useful. Genetics and health Resources for Patients and Families Resources for Health Professionals What glossary definitions help with understanding CPT II deficiency? acids ; arrhythmia ; autosomal ; autosomal recessive ; breakdown ; cardiomyopathy ; carnitine ; cell ; coma ; deficiency ; enzyme ; fasting ; fatty acids ; ...
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