Lambert Eaton myasthenic syndrome (LEMS): clinical features
Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .
Lambert Eaton myasthenic syndrome (LEMS): clinical features. LEMS is an autoimmune disorder of the neuromuscular junction.
Pathology
- LEMS is an autoimmune disorder of the neuromuscular junction
- It is caused by autoantibodies to voltage-gated calcium channels (VGCCs)
- It is paraneoplastic in 50-60% of cases
- Non-paraneoplastic LEMS is often associated with HLA B8, DR3 and DQ2
Limb weakness
Locked: subscribe to see this section.
Ptosis
Locked: subscribe to see this section.
Other neuromuscular features
Locked: subscribe to see this section.
Autonomic features
Locked: subscribe to see this section.
Associated autoimmune disorders
Locked: subscribe to see this section.
Differential diagnosis: myasthenia gravis (MG)
Locked: subscribe to see this section.
Differential diagnoses: others
Locked: subscribe to see this section.
Acronym
Locked: subscribe to see this section.
References
- Gilhus NE. Lambert-eaton myasthenic syndrome; pathogenesis, diagnosis, and therapy. Autoimmune Dis 2011; 2011:973808.
- Mareska M, Gutmann L. Lambert-Eaton syndrome. Semin Neurol 2004; 24:149-153.
- Titulaer MJ, Lang B, Verschuuren JJGM. Lambert-Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies. Lancet 2011; 10:1098-1107.
- Weimer MB, Wong J. Lambert-eaton myasthenic syndrome. Curr Treat Options Neurol 2009; 11:77-84.
- Sabater L, Titulaer M, Saiz A, Verschuuren J, Gure AO, Graus F. SOX1 antibodies are makers of paraneoplastic Lambert-Eaton myasthenic syndrome. Neurology 2008; 70:924-928.
- And 7 more. Subscribe to see the full list