Dural graft-associated Creutzfeldt-Jakob Disease (Q87908): Difference between revisions
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Doença de Creutzfeldt-Jakob associada a enxerto dural (DCJd) que se desenvolve em pacientes transplantados com dura de cadáver humano que tinha o príon "infeccioso". Foi descrita pela primeira vez em 1972 e mais tarde foi relatada principalmente no Japão. Após os tratamentos químicos especiais da dura-máter e a proibição do uso da dura-máter de cadáveres em qualquer circunstância, a ocorrência de dCJD diminuiu drasticamente nos anos subsequentes. | |||
| description / en | description / en | ||
Dural graft-associated Creutzfeldt-Jakob Disease (dCJD) developed in patients transplanted with human cadaveric dura that had the "infectious" prion. It was first described in 1972 and later has been reported mainly in Japan. After the special chemical treatments of the dura and prohibition of use of cadaveric dura in general, dCJD occurrence has dramatically decreased in subsequent years. | |||
Revision as of 13:57, 15 August 2026
Dural graft-associated Creutzfeldt-Jakob Disease (dCJD) developed in patients transplanted with human cadaveric dura that had the "infectious" prion. It was first described in 1972 and later has been reported mainly in Japan. After the special chemical treatments of the dura and prohibition of use of cadaveric dura in general, dCJD occurrence has dramatically decreased in subsequent years.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_70256049 |
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| English | Dural graft-associated Creutzfeldt-Jakob Disease |
Dural graft-associated Creutzfeldt-Jakob Disease (dCJD) developed in patients transplanted with human cadaveric dura that had the "infectious" prion. It was first described in 1972 and later has been reported mainly in Japan. After the special chemical treatments of the dura and prohibition of use of cadaveric dura in general, dCJD occurrence has dramatically decreased in subsequent years. |
