Fatal familial insomnia (Q38207): Difference between revisions
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Doença do cérebro, causada pela herança de mutação(ões) de genes normais da proteína priônica. Essa doença é caracterizada por insônia severa e disfunção do sistema autônomo e é fatal. A confirmação é feita por meio de exame patológico do cérebro e teste genético. | |||
| description / en | description / en | ||
A disease of the brain, caused by inheritance of mutation(s) of normal prion protein genes. This disease is characterised by severe insomnia and autonomic system dysfunction, and is fatal. Confirmation is by pathological examination of the brain and genetic testing. | |||
Revision as of 02:56, 13 August 2026
A disease of the brain, caused by inheritance of mutation(s) of normal prion protein genes. This disease is characterised by severe insomnia and autonomic system dysfunction, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8E02.2 |
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| English | Fatal familial insomnia |
A disease of the brain, caused by inheritance of mutation(s) of normal prion protein genes. This disease is characterised by severe insomnia and autonomic system dysfunction, and is fatal. Confirmation is by pathological examination of the brain and genetic testing. |
