Certain specified neurological disorder aquaporin-4 antibody positive (Q84139): Difference between revisions

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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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Latest revision as of 09:30, 15 August 2026

Since discovery of the neural autoantibody to aquaporin-4 (AQP4-IgG) as a biomarker of neuromyelitis optica a wider spectrum of neurological disease associated with AQP4-IgG seropositivity is recognised and often referred to as NMO spectrum disorders (see NMO spectrum disorders [NMOSD] definition), but may be categorized under this heading emphasizing disease outside the optic nerves and spinal cord. This includes nausea/vomiting attacks from area postrema lesions, syndrome of inappropriate anti-diuretic-hormone secretion (SIADH) or narcolepsy from hypothalamic lesions, posterior reversible encephalopathy syndrome (PRES) or acute disseminated encephalomyelitis (ADEM) like presentations from cerebral involvement and myositis from muscle involvement.
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ID_31533652
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    Certain specified neurological disorder aquaporin-4 antibody positive
    Since discovery of the neural autoantibody to aquaporin-4 (AQP4-IgG) as a biomarker of neuromyelitis optica a wider spectrum of neurological disease associated with AQP4-IgG seropositivity is recognised and often referred to as NMO spectrum disorders (see NMO spectrum disorders [NMOSD] definition), but may be categorized under this heading emphasizing disease outside the optic nerves and spinal cord. This includes nausea/vomiting attacks from area postrema lesions, syndrome of inappropriate anti-diuretic-hormone secretion (SIADH) or narcolepsy from hypothalamic lesions, posterior reversible encephalopathy syndrome (PRES) or acute disseminated encephalomyelitis (ADEM) like presentations from cerebral involvement and myositis from muscle involvement.

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      CID11:ID_31533652
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      dki-india-ID_31533652
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      Concluído
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      13 August 2026
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