Najjar syndrome revisited

Am J Med Genet. 1993 Dec 1;47(8):1151-2. doi: 10.1002/ajmg.1320470803.

Abstract

We describe 2 brothers with cardiomyopathy and hypergonadotropic hypogonadism and conclude that this is the first description of the Najjar syndrome in the United States. The inheritance may be autosomal recessive.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cardiomyopathies / genetics*
  • Humans
  • Hypogonadism / genetics*
  • Infant, Newborn
  • Male
  • Syndrome