| Literature DB >> 945511 |
C Angelini, S Lücke, F Cantarutti.
Abstract
We studied a 10-year-old girl with an insidious muscle disease beginning at age 7. Muscle biopsy showed that the majority of type I fibers were vacuolated and contained lipid excess. Carnitine deficiency was found in skeletal muscle. The patient was treated with 3.0 gm L-carnitine per day and with a medium-chain triglyceride diet. She showed a rapid improvement and recovery of strength. A muscle biopsy 8 months later showed a decreased lipid content. Oral carnitine replacement represents an effective treatment for the disease.Entities:
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Year: 1976 PMID: 945511 DOI: 10.1212/wnl.26.7.633
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910