Table 1.

Key features of syndromes associated with neuronal surface antibodies

AntibodyDemographicsKey distinguishing featuresTumour associations
Age predominanceF:M ratio
NMDARChildren and adults <40 years4:1Psychiatric features followed by movement disorder (classically orofacial dyskinesia), seizures, encephalopathy and autonomic dysfunctionAbout 50% of female patients have ovarian teratoma; other tumour associations have been described
LGI1Older adults1:2Faciobrachial dystonic seizures, amnesia, hyponatraemia<10%: breast, lymphoma, thymoma, thyroid
CASPR2Older adults1:9Sleep disorders (insomnia, sleep-wake cycle disturbance), peripheral nerve hyperexcitability, ataxia<5%: various tumours
GABAARChildren or adults1:1Seizures30%: thymoma
GABABROlder adults1:1.5Seizures, amnesia50%: SCLC
AMPAROlder adults2:1Amnesia65%: breast, SCLC, thymoma
DPPXAdults1:2Severe diarrhoea and weight loss, myoclonus, hyperekplexia<10%: lymphoma
  • AMPAR = α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor; CASPR2 = contactin-associated protein-like 2; DPPX = dipeptidyl-peptidase-like protein 6; GABAAR = γ-aminobutyric acid type A receptor; GABABR = γ-aminobutyric acid type B receptor; LGI1 = leucine-rich glioma-inactived 1; NMDAR = N-methyl-D-aspartate receptor; SCLC = small cell lung cancer.