loading...| Preferred Name | Reye syndrome | |
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| Definitions |
A rare, systemic disease characterized by persistent vomiting with confusion, lethargy, disorientation, hyperreflexia, hyperventilation, and tachycardia, with rapid progression to seizures, non-inflammatory encephalopathy, coma and death. It typically develops between 12 hours and 3 weeks after recovery from a viral illness, such as upper respiratory tract infection or gastroenteritis. Hepatomegaly, acute hepatic steatosis, fatty liver degeneration and multiple laboratory abnormalities are associated. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_3096 |
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| definition |
A rare, systemic disease characterized by persistent vomiting with confusion, lethargy, disorientation, hyperreflexia, hyperventilation, and tachycardia, with rapid progression to seizures, non-inflammatory encephalopathy, coma and death. It typically develops between 12 hours and 3 weeks after recovery from a viral illness, such as upper respiratory tract infection or gastroenteritis. Hepatomegaly, acute hepatic steatosis, fatty liver degeneration and multiple laboratory abnormalities are associated. |
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| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=3096 |
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| hasDbXref |
MeSH:D012202 MedDRA:10039012 ICD-11:8E46 UMLS:C0035400 ICD-10:G93.7 |
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| label |
Reye syndrome |
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| notation |
ORPHA:3096 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_3096 |
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| prefLabel |
Reye syndrome |
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| subClassOf |