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Biochemical and Morphological Studies on a Case of Systemic Carnitine Deficiency

  • C. Cerri
  • G. Meola
  • G. Scarlato
Part of the Acta Neuropathologica Supplementum book series (NEUROPATHOLOGIC, volume 7)

Summary

The authors report a patient with systemic carnitine deficiency in which, despite restoration of normal serum carnitine level by therapy, the fatal course of the disease progressed. Postmortem studies of cardiac muscle with Oil red O failed to show lipid accumulation which was still present in muscle and liver. Carnitine level in liver was less than 10% of the controls values; total carnitine in muscle was 50% of the controls with differences in its esterification pattern: whereas the free carnitine was 1/10 of normal, the long chain esterified one was 3 times higher than the control. Heart carnitine content was normal. The authors suggest that although no therapeutic effects were detected in skeletal muscle, the normal carnitine content and the absence of lipidosis in the heart suggest that carnitine therapy may have been beneficial in our patient enabling the heart to utilize fatty acids.

Key words

carnitine deficiency lipidosis replacement therapy 

References

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Copyright information

© Springer-Verlag 1981

Authors and Affiliations

  • C. Cerri
    • 1
  • G. Meola
    • 2
  • G. Scarlato
    • 2
  1. 1.H. Houston Merritt Clinical Research Center for Muscular Dystrophy and Related DiseasesColumbia UniversityNew YorkUSA
  2. 2.Department of Neurology, Medical SchoolUniversity of MilanMilanItaly

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