loading...| Preferred Name | Miller Fisher syndrome | |
| Synonyms |
Fisher syndrome Cranial variant of Guillain-Barré syndrome Cranial variant of GBS |
|
| Definitions |
A rare acquired peripheral neuropathy characterized by acute ophthalmoplegia, ataxia, and areflexia, typically manifesting with diplopia and unsteady gait, and generalized areflexia. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_98919 |
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| alternative_term |
Fisher syndrome Cranial variant of Guillain-Barré syndrome Cranial variant of GBS |
|
| definition |
A rare acquired peripheral neuropathy characterized by acute ophthalmoplegia, ataxia, and areflexia, typically manifesting with diplopia and unsteady gait, and generalized areflexia. |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=98919 |
|
| has_age_of_onset |
All ages |
|
| has_inheritance |
Not applicable Multigenic/multifactorial |
|
| hasDbXref |
MedDRA:10049567 UMLS:C0393799 ICD-10:G61.0 MeSH:D019846 ICD-11:8C01.0 |
|
| label |
Miller Fisher syndrome |
|
| notation |
ORPHA:98919 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_98919 |
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| prefLabel |
Miller Fisher syndrome |
|
| present_in |
Europe AND has_annual_incidence_average_value : 0.1 AND has_annual_incidence_range : 1-9 / 1 000 000 Europe AND has_point_prevalence_range : 1-9 / 1 000 000 |
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| treeView | ||
| subClassOf |