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Results 1 - 10 of 19 for Family history of cardiomyopathy
  1. ... Hypertrophic cardiomyopathy also occurs in people with no family history; these cases are considered nonfamilial hypertrophic cardiomyopathy. In familial hypertrophic cardiomyopathy, cardiac thickening usually occurs ...
  2. ... altered gene never develop features of familial dilated cardiomyopathy. (This situation is known as reduced penetrance.) Other cases result from new mutations in the gene and occur in people with no history of the disorder in their family.In rare instances, this condition is inherited in ...
  3. ... of inheritance, although many affected individuals have a family history of problems with alcohol or other substances. Children of people with alcohol use disorder are two to six times more likely than the general public to develop alcohol ... Genetic Testing Registry: ...
  4. ... mitochondrial gene and occurs in people with no family history of MERRF. Fukuhara disease MERRF MERRF syndrome Myoclonic ...
  5. ... variants that occur spontaneously, and there is no family history of this condition. Infantile subacute necrotizing encephalopathy Juvenile ...
  6. ... White syndrome occur in people with no apparent family history of the condition. These cases are described as ...
  7. ... the gene and occur in people with no history of caveolinopathies in their family. Elevated serum CPK Elevated serum creatine phosphokinase H- ...
  8. ... the gene and occur in people with no history of caveolinopathies in their family. Distal myopathy, Tateyama type MPDT Genetic Testing Registry: ...
  9. ... the gene and occur in people with no history of caveolinopathies in their family.Autosomal recessive inheritance means that both copies of ...
  10. ... early embryonic development. These affected individuals have no history of the disorder in their family. Faciocutaneoskeletal syndrome FCS syndrome Genetic Testing Registry: Costello ...
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