LP420677-9
IgLON family member 5 Ab.IgG
Active
Description
IgLON family member 5 (IgLON5) is a neural cell adhesion protein encoded by the gene IGLON5. Anti-IgLON5 disease is associated with autoantibodies against IgLON5. Symptoms include sleep disturbances such as vocalizations, movements, stridor, and obstructive sleep apnea, as well as problems with gait, swallowing, speech, oculomotor function, and cognition. The disease affects both sexes equally, and typical onset is after the age of 50. Patients with anti-IgLON5 disease usually have anti-IgLON antibodies in both serum and CSF specimens. PMID: 30694925 Source: Regenstrief LOINC
Basic Part Properties
- Part Display Name
- IgLON5 IgG
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2020-10-24
- Construct for LOINC Short Name
- IgLON5 IgG
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LOINC Copyright
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