Opsoclonus-myoclonus syndrome

Disease ID:1137
Name:Opsoclonus-myoclonus syndrome
Associated with:1 target
Synonyms
dancing eye syndrome | Kinsbourne syndrome | OMA syndrome | paraneoplastic opsoclonus-myoclonus | paraneoplastic opsoclonus-myoclonus-ataxia
Description
Opsoclonus myoclonus syndrome (OMS) is a rare pediatric brain inflammatory disease of paraneoplastic, parainfectious or idiopathic origin, characterized by opsoclonus, myoclonus, ataxia and behavioural and sleep disorders.
Database Links
Orphanet: ORPHA1183

Targets

CXCR5
References:  1

Ligands

No ligand related data available for Opsoclonus-myoclonus syndrome

References

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1. Pranzatelli MR, Tate ED, McGee NR, Travelstead AL, Ransohoff RM, Ness JM, Colliver JA. (2012) Key role of CXCL13/CXCR5 axis for cerebrospinal fluid B cell recruitment in pediatric OMS. J. Neuroimmunol., 243 (1-2): 81-8. [PMID:22264765]