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Results 1 - 10 of 33 for Familial restrictive cardiomyopathy
  1. Familial dilated cardiomyopathy is a genetic form of heart disease. It occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of ...
  2. ... S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. ...
  3. Hypertrophic cardiomyopathy is a heart condition characterized by thickening (hypertrophy) of the heart (cardiac) muscle. When multiple members of a family have the ...
  4. ... HAIR AND KERATODERMA; DCWHK ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11 CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; ...
  5. ... Jacobson Z, Young TL, Marshall JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alstrom syndrome: a report of four sibs. ...
  6. ... DYSPLASIA, FAMILIAL, 11; ARVD11 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13 PubMed Corrado D, Link MS, Calkins H. Arrhythmogenic Right Ventricular Cardiomyopathy. N Engl J Med. 2017 Jan 5;376( ...
  7. ... their genetic cause. The most common form of familial partial lipodystrophy ... muscle (cardiomyopathy), a form of heart disease called coronary artery ...
  8. ... this condition have short stature compared to their family and peers and may have ... Neurological problems in people with Costello syndrome include ...
  9. Early-onset myopathy with fatal cardiomyopathy (EOMFC) is an inherited muscle disease that affects the skeletal muscles, which are used for movement, and the ...
  10. ... by catecholamines Catecholamine-induced polymorphic ventricular tachycardia CPVT Familial polymorphic ventricular tachycardia FPVT ... PubMed ...
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