Neuromyelitis optica spectrum disorder (NMOSD): systemic features
Evidence-based neurology checklist on neuromyelitis optica spectrum disorder (nmosd): systemic features: Endocrine Morbid obesity Hyperinsulinaemia Hyperandrogenism Amenorrhoea Galactorrhoea Hyponatraemia Panhypopituitarism Paraneoplastic Obstetric Autoimmune associations Other systemic NMO…
Endocrine
- Morbid obesity
- Hyperinsulinaemia
- Hyperandrogenism
- Amenorrhoea
- Galactorrhoea
- Hyponatraemia
- Panhypopituitarism
Paraneoplastic
Obstetric
Autoimmune associations
Other systemic NMO associations
Possible infective triggers for NMO
References
- Hacohen Y, Messina S, Gan HW, et al. Endocrinopathies in paediatric-onset neuromyelitis optica spectrum disorder with aquaporin 4 (AQP4) antibody. Mult Scler 2017; 1:1352458517726593 (Epub ahead of print).
- Shahmohammadi S, Doosti R, Shahmohammadi A, et al. Autoimmune diseases associated with neuromyelitis optica spectrum disorders: a literature review. Mult Scler Relat Disord 2018; 27:350-363.
- Watanabe M, Furusho K, Takahashi T, Tamaoka A. Galactorrhea in a patient with aquaporin-4 qntibody-positive neuromyelitis optica spectrum disorder: a case report and review of the literature. Neurologist 2015; 20:101-103.
- Jin S, Long Z, Wang W, Jiang B. Hyponatremia in neuromyelitis optica spectrum disorders: literature review. Acta Neurol Scand 2018; 138:4-11.
- Dixon-Douglas J, Burgess J, Dreyer M. Hypothalamic demyelination causing panhypopituitarism. Intern Med J 2018; 48:580-582.
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Related checklists
- Neuromyelitis optica spectrum disorders (NMOSD): diagnostic criteria
- Neuromyelitis optica spectrum disorder (NMOSD): central neurological features
- Neuromyelitis optica spectrum disorder (NMOSD): peripheral neurological features
- Neuromyelitis optica spectrum disorder (NMOSD): paraneoplastic
- Neuromyelitis optica spectrum disorder (NMOSD): area postrema syndrome (APS)
- Neuromyelitis optica spectrum disorder (NMOSD): clinical differentials
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