Late onset dilated cardiomyopathy in a unique familial syndrome of hypogonadism and metabolic abnormalities
- 1 December 1987
- journal article
- case report
- Published by Elsevier BV in American Heart Journal
- Vol. 114 (6), 1522-1524
- https://doi.org/10.1016/0002-8703(87)90561-8
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intoleranceAmerican Journal Of Medicine, 1976
- Familial Syndrome of Primary Testicular Insufficiency with Normal Virilization, Blindness, Deafness and Metabolic AbnormalitiesNew England Journal of Medicine, 1969
- Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden deathAmerican Heart Journal, 1957