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Asymptomatic dystrophinopathy

A Morrone1, E Zammarchi, P C Scacheri

  • 1Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pennsylvania 15261, USA.

American Journal of Medical Genetics
|March 31, 1997
PubMed
Summary
This summary is machine-generated.

This study identifies asymptomatic dystrophinopathy in multiple males, challenging presymptomatic diagnoses of Becker muscular dystrophy based solely on genetic findings.

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Area of Science:

  • Genetics
  • Neurology
  • Molecular Biology

Background:

  • Mild, persistent elevation of serum aspartate aminotransferase (AST) and creatine kinase (CK) can indicate underlying neuromuscular conditions.
  • Carrier states for muscular dystrophies are typically identified through genetic and protein analysis.