Reye Syndrome and Reye-Like Syndrome

Pediatric Neurology

Volumn 39, Issue 3, 2008, Pages 198-200

  Gosalakkal, Jayaprakash A ^a   Kamoji, Vishwanath ^a  

^a LEICESTER ROYAL INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLSALICYLIC ACID; ALANINE AMINOTRANSFERASE; BENZOIC ACID; CARNITINE; GLUCOSE; LONG CHAIN ACYL COENZYME A DEHYDROGENASE; MANNITOL;

ADOLESCENT; ALANINE AMINOTRANSFERASE BLOOD LEVEL; AMMONIA BLOOD LEVEL; ANAMNESIS; ARTICLE; ARTIFICIAL VENTILATION; BLOOD GAS; BRAIN EDEMA; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; CONFUSION; DEATH; DECREASED APPETITE; DETERIORATION; DIFFERENTIAL DIAGNOSIS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DISORIENTATION; ELECTROCARDIOGRAM; ELECTROENCEPHALOGRAM; ENZYME ACTIVITY; ENZYME DEFICIENCY; FEMALE; FEVER; FIBROBLAST CULTURE; HEART MUSCLE ISCHEMIA; HEPATOMEGALY; HOSPITAL ADMISSION; HUMAN; HYPERAMMONEMIA; LABORATORY TEST; METABOLIC DISORDER; MULTIPLE ORGAN FAILURE; MUSCLE HYPERTONIA; PATHOGENESIS; PHYSICAL EXAMINATION; PRIORITY JOURNAL; REYE LIKE SYNDROME; REYE SYNDROME; THETA RHYTHM; VOMITING;

ACYL-COA DEHYDROGENASE, LONG-CHAIN; ADOLESCENT; FEMALE; HUMANS; LIPID METABOLISM, INBORN ERRORS; MITOCHONDRIA, LIVER; REYE SYNDROME;

EID: 49749096404     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2008.06.003     Document Type: Article

References (13)

1. Reye R.D., Morgan G., and Baral J. Encephalopathy and fatty degeneration of the viscera: A disease entity in childhood. Lancet 2 (1963) 749-752
2. Casteels-Van Daele M., Van Geet C., Wouters C., and Eggermont E. Reye syndrome revisited: Descriptive term covering a group of heterogeneous disorders. Eur J Pediatr 159 (2002) 641-648
3. Saudubray J.M., Martin D., de Lonlay P., et al. Recognition and management of fatty acid oxidation defects: A series of 107 patients. Inherit Metab Dis 22 (1999) 488-502
4. Lyon G., Adams R.D., and Kolodony E.H. Early infantile progressive metabolic encephalopathies. In: Lyon G., Adams R.D., and Kolodony E.H. (Eds). Neurology of hereditary metabolic diseases of children (1996), McGraw-Hill, New York 108-109
5. Calvani M. Reye's syndrome: The death of a syndrome (or death by a syndrome)?. Recenti Prog Med 91 (2000) 675-680
6. Vianey-Liaud C., Dairy P., Gregersen N., and Mathieu M. The inborn errors of mitochondrial fatty acid oxidation. J Inherit Metab Dis 10 (1987) 159-200
7. Indo Y., Coates P.M., Hale D.E., and Tanaka K. Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency. Pediatr Res 30 (1991) 211-215
8. Cox K.B., Hamm D.A., Millington D.S., et al. Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse. Hum Mol Genet 10 (2001) 2069-2077
9. Zhang D., Liu Z.X., Choi C.S., et al. Molecular characterization of inherited medium chain acyl co A dehydrogenase deficiency. Proc Natl Acad Sci USA 104 (2007) 17075-17080
10. Bhutta A.T., Van Savell H., and Schexnayder S.M. Reye's syndrome: Down but not out. South Med J 96 (2003) 43-45
11. Casteels-Van Daele M., Van Geet C., Wouters C., and Eggermont E. Reye syndrome revisited: A descriptive term covering a group of heterogeneous disorders. Eur J Pediatr 159 (2000) 641-648
12. You K. Salicylate and mitochondrial injury in Reye's syndrome. Science 221 (1983) 163-165
13. Caotes P.M. New developments in the diagnosis and investigation of mitochondrial fatty acid oxidation. Eur J Pediatr 153 Suppl. (1994) S49-S56