X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060

J Pediatr. 1999 Sep;135(3):273-6. doi: 10.1016/s0022-3476(99)70118-6.
No abstract available

Publication types

  • Comment
  • Editorial
  • Review

MeSH terms

  • Cardiomyopathy, Dilated / diagnosis
  • Cardiomyopathy, Dilated / genetics*
  • Cardiomyopathy, Dilated / metabolism
  • Child
  • Genetic Linkage / genetics*
  • Glutarates / urine*
  • Growth Disorders / diagnosis
  • Growth Disorders / genetics*
  • Growth Disorders / metabolism
  • Humans
  • Male
  • Mitochondrial Myopathies / diagnosis
  • Mitochondrial Myopathies / genetics*
  • Mitochondrial Myopathies / metabolism
  • Mutation / genetics
  • Neutropenia / diagnosis
  • Neutropenia / genetics*
  • Neutropenia / metabolism
  • Syndrome
  • X Chromosome / genetics*

Substances

  • Glutarates
  • 3-methylglutaconic acid