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Peripheral Neuropathy and Amyotrophic Lateral Sclerosis

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Neuro-Geriatrics

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).

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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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Correspondence to Erik P. Pioro M.D., Ph.D. .

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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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  • DOI: https://doi.org/10.1007/978-3-319-56484-5_16

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