Abstract
This chapter covers two groups of disorders that share a common anatomical substrate (the peripheral nervous system), but are strikingly different in their biology, prevalence, clinical presentations, and prognosis. Polyneuropathy is common, affects up to 8% of the population older than 50 years (J Neurol Neurosurg Psychiatry 62:310–318, 1997), is diverse in its cause (often symptomatic of a underlying systemic disorder such as diabetes), often presents with sensory symptoms or pain, and usually has a chronic benign course. Amyotrophic lateral sclerosis, on the other hand, is an uncommon although not rare (lifetime risk about 1/400) (Eur J Neurol 16:745–751, 2009) relatively homogenous primary neurodegeneration that largely manifests with muscle weakness/atrophy, and is fatal (median survival is about 3 years).
Abbreviations
- ALS:
-
Amyotrophic lateral sclerosis
- CIAP:
-
Chronic idiopathic axonal polyneuropathy
- CIDP:
-
Chronic inflammatory demyelinating polyradiculoneuropathy
- CMT:
-
Charcot-Marie-Tooth syndrome
- DSP:
-
Distal symmetric polyneuropathy
- EDX:
-
Electrodiagnostic testing
- FAP:
-
Familial amyloid polyneuropathy
- FVC:
-
Forced vital capacity
- GBS:
-
Guillain-Barré syndrome
- GTT:
-
Glucose tolerance test
- HNPP:
-
Hereditary neuropathy with liability to pressure palsies
- IGT:
-
Impaired glucose tolerance
- LMN:
-
Lower motor neuron
- MAG:
-
Myelin-associated glycoprotein
- MGUS:
-
Monoclonal gammopathy of undetermined significance
- MMN:
-
Multifocal motor neuropathy
- NIPPV:
-
Non-invasive positive pressure ventilation
- PEG:
-
Percutaneous endoscopic gastrostomy
- RLS:
-
Restless legs syndrome
- SNRI:
-
Serotonin norepinephrine reuptake inhibitor
- TCA:
-
Tricyclic antidepressant
- TTR:
-
Transthyretin
- UMN:
-
Upper motor neuron
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Thakore, N.J., Pioro, E.P. (2017). Peripheral Neuropathy and Amyotrophic Lateral Sclerosis. In: Tousi, B., Cummings, J. (eds) Neuro-Geriatrics. Springer, Cham. https://doi.org/10.1007/978-3-319-56484-5_16
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