| Literature DB >> 6401355 |
A E Slonim, R A Coleman, M A McElligot, J Najjar, K Hirschhorn, G U Labadie, R Mrak, O B Evans, E Shipp, R Presson.
Abstract
Progressive muscle weakness in acid maltase deficiency (AMD) is associated with intralysosomal accumulation of glycogen and altered myofibrillar morphology. A rapid fall in circulating branched chain amino acids after protein ingestion in a child with AMD suggested that increased net muscle protein catabolism may play a part in the pathogenesis of this condition. To reduce this muscle catabolism, the patient was treated with a high-protein diet for 12 months. This has reversed the weakness and wasting, with improvement in muscle function, exercise tolerance, and growth.Entities:
Mesh:
Substances:
Year: 1983 PMID: 6401355 DOI: 10.1212/wnl.33.1.34
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910