Myelitis due to schistosoma species (Q86633): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Distúrbio inflamatório da medula espinal devido à infecção por uma espécie esquistossomótica. Os sintomas e sinais podem ser agudos ou subagudos no início e incluem paraparesia ou paraplegia, perda sensorial apropriada com o nível da medula espinhal afetada, perda do controle do esfíncter e sinais do neurônio motor inferior. O diagnóstico pode ser confirmado por neuroimagem, análise do líquido espinal, testes sorológicos e biópsia | |||
| description / en | description / en | ||
An inflammatory disorder of the spinal cord due to infection by a schistosomal species. The symptoms and signs may be acute or subacute in onset, and include paraparesis or paraplegia, sensory loss appropriate with the level of the spinal cord affected, loss of sphincter control, and lower motor neurone signs. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis, serological tests, and biopsy. | |||
Revision as of 12:04, 15 August 2026
An inflammatory disorder of the spinal cord due to infection by a schistosomal species. The symptoms and signs may be acute or subacute in onset, and include paraparesis or paraplegia, sensory loss appropriate with the level of the spinal cord affected, loss of sphincter control, and lower motor neurone signs. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis, serological tests, and biopsy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_37486018 |
||
| English | Myelitis due to schistosoma species |
An inflammatory disorder of the spinal cord due to infection by a schistosomal species. The symptoms and signs may be acute or subacute in onset, and include paraparesis or paraplegia, sensory loss appropriate with the level of the spinal cord affected, loss of sphincter control, and lower motor neurone signs. Diagnosis may be confirmed by neuroimaging, spinal fluid analysis, serological tests, and biopsy. |
