Familial Cardiomyopathy, Hypogonadism, and Collagenoma

  1. HARVEY N. SACKS, M.D.;
  2. I. SYLVIA CRAWLEY, M.D.;
  3. JOHN A. WARD, M.D.; and
  4. ROBERT M. FINE, M.D.
  1. Decatur and Atlanta, Georgia

    Abstract

    A patient with tricuspid regurgitation by clinical evaluation, cardiac catheterization, and angiography was found at autopsy to have a cardiomyopathy involving both ventricles but with predominant involvement of the right ventricle. He also had primary testicular failure and a distinctive type of collagenoma. The patient's two brothers were examined and found to have similar collagenomas and testicular failure. Evidence for a mild to moderate degree of cardiomyopathy was also apparent by findings on physical examination, chest roentgenogram, electrocardiogram, and echocardiogram. The father was known to have had a similar skin lesion and congestive heart failure. The aspects of the clinical presentation of this patient and the findings in the two brothers are discussed. A common genetic link in this familial syndrome is not elucidated.

    Article and Author Information

    • ▸From the Medical and Dermatology Services, Atlanta Veterans Administration Medical Center, Decatur, Georgia; and the Departments of Medicine and Dermatology, Emory University School of Medicine, Atlanta, Georgia.

    • ▸Requests for reprints should be addressed to I. Sylvia Crawley, M.D.; Veterans Administration Medical Center, 1670 Clairmont Road; Decatur, GA 30033.

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