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Related Experiment Videos

Najjar syndrome revisited

I T Thomas1, T Jewett, P Lantz

  • 1Department of Pediatrics, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina 27157-1081.

American Journal of Medical Genetics
|December 1, 1993
PubMed
Summary

This study details Najjar syndrome, a rare condition involving cardiomyopathy and hypergonadotropic hypogonadism, observed in two brothers. This marks the first documented U.S. case, suggesting potential autosomal recessive inheritance.

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Area of Science:

  • Cardiology
  • Genetics
  • Endocrinology

Background:

  • Najjar syndrome is a rare genetic disorder.
  • It is characterized by cardiomyopathy and hypergonadotropic hypogonadism.
  • Previous cases have not been documented in the United States.