Najjar syndrome revisited.

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.

• Authors: I T Thomas, T Jewett, P Lantz, W Covitz, P Garber, M N Berry
• Journal: American journal of medical genetics (Am J Med Genet) Vol. 47 Issue 8 Pg. 1151-2 (Dec 01 1993) ISSN: 0148-7299 [Print] United States
• PMID: 8291546 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)

Topics

• Cardiomyopathies (genetics)
• Humans
• Hypogonadism (genetics)
• Infant, Newborn
• Male
• Syndrome