Reye's syndrome; diagnosis by muscle biopsy?

Author:

Shapira Y,Deckelbaum R,Statter M,Tennenbaum A,Aker M,Yarom R

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference7 articles.

1. Acute encephalopathy with fatty infiltration of the viscera;C, Devivo D.; P, Keating J.; W, Haymond M.;Pediatr Clin North Am,1976

2. Recurrent Reye's syndrome;E, Pichichero M.; B, McCabe E.R.;Am J Dis Child; Letter: Reye's syndrome-virus or artefact in muscle,1978

3. Ultrastructural lesions of muscle and immunofluorescent deposits in vessels in Reye's syndrome. A preliminary report of muscle biopsies;A, Hanson P.; E, Urizar R.;Ann Neurol,1977

4. Willems One can speculate that the cause of the accumulation of lipids inside the hepatocytes and myofibres in our patients was a result of the mitochondrial damage and lack of ability to oxidise the lipids;A, Sengers R.C.; ter Haar B G; F, Trijbels J.M.;J Pediatr; Daniels 0, Stadhouders A M. Congenital cataract and mitochondrial myopathy of skeletal and heart muscle associated with lactic acidosis after exercise,1975

5. Carnitine deficiency of human evidence to support the suggestion that Reye's syndrome can be regarded as a specific mitochondriopathy is given by the enzymatic studies of the urea cycle in the liver biopsy. In Case 1 low enzymatic skeletal muscle with associated lipid storage myopathy. A new syndrome;G, Engel A.; C, Angelini;Science,1973

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