Cerebrofacial arteriovenous metameric syndrome type 2 (Q100736): Difference between revisions
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A síndrome de Wyburn-Mason ou síndrome de Bonnet-Dechaume-Blanc é caracterizada pela associação de malformações arteriovenosas de maxila, retina, nervo óptico, tálamo, hipotálamo e córtex cerebral. | |||
| description / en | description / en | ||
Wyburn-Mason syndrome or Bonnet-Dechaume-Blanc syndrome is characterised by the association of arteriovenous malformations of the maxilla, retina, optic nerve, thalamus, hypothalamus and cerebral cortex. | |||
Revision as of 17:28, 16 August 2026
Wyburn-Mason syndrome or Bonnet-Dechaume-Blanc syndrome is characterised by the association of arteriovenous malformations of the maxilla, retina, optic nerve, thalamus, hypothalamus and cerebral cortex.
| Language | Label | Description | Also known as |
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| default for all languages | ID_2044557254 |
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| English | Cerebrofacial arteriovenous metameric syndrome type 2 |
Wyburn-Mason syndrome or Bonnet-Dechaume-Blanc syndrome is characterised by the association of arteriovenous malformations of the maxilla, retina, optic nerve, thalamus, hypothalamus and cerebral cortex. |
