Dysplastic cerebellar gangliocytoma (Q53244): Difference between revisions
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Gangliocitoma displásico cerebelar (doença de Lhermitte-Duclos) é um transtorno muito raro, caracterizado pelo desenvolvimento anormal e aumento do cerebelo, e aumento da pressão intracraniana. Manifesta-se com cefaleia, náusea, disfunção cerebelar, hidrocefalia oclusiva, ataxia, distúrbios visuais e paralisia de outros nervos cranianos. | |||
| description / en | description / en | ||
Dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease) is a very rare disorder characterised by abnormal development and enlargement of the cerebellum, and an increased intracranial pressure and manifests with headache, nausea, cerebellar dysfunction, occlusive hydrocephalus, ataxia, visual disturbances and other cranial nerve palsies. | |||
Revision as of 00:40, 14 August 2026
Dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease) is a very rare disorder characterised by abnormal development and enlargement of the cerebellum, and an increased intracranial pressure and manifests with headache, nausea, cerebellar dysfunction, occlusive hydrocephalus, ataxia, visual disturbances and other cranial nerve palsies.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1557864133 |
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| English | Dysplastic cerebellar gangliocytoma |
Dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease) is a very rare disorder characterised by abnormal development and enlargement of the cerebellum, and an increased intracranial pressure and manifests with headache, nausea, cerebellar dysfunction, occlusive hydrocephalus, ataxia, visual disturbances and other cranial nerve palsies. |
