
Michael Johnston, MD
et al.
Published online:
01 March 2017
Published in print:
01 August 2016
Online ISBN:
9780190219093
Print ISBN:
9780199937837
Contents
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Introduction Introduction
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Autoimmune Autonomic Ganglionopathy Autoimmune Autonomic Ganglionopathy
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Guillain-Barre Syndrome Guillain-Barre Syndrome
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Porphyria Porphyria
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Drug Induced Acute Autonomic Neuropathies Drug Induced Acute Autonomic Neuropathies
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Heavy Metal Poisoning Heavy Metal Poisoning
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Morvan’s Syndrome Morvan’s Syndrome
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Distal Small Fiber Neuropathy Distal Small Fiber Neuropathy
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Lambert Eaton Myasthenic Syndrome Lambert Eaton Myasthenic Syndrome
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Chronic Idiopathic Anhidrosis Chronic Idiopathic Anhidrosis
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Chagas’ Disease Chagas’ Disease
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Amyloid Neuropathy Amyloid Neuropathy
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Sensory Neuronopathy with Autonomic Failure Sensory Neuronopathy with Autonomic Failure
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Familial Dysautonomia Familial Dysautonomia
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Hereditary Sensory Neuropathy Hereditary Sensory Neuropathy
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Adrenomyeloneuropathy Adrenomyeloneuropathy
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Fabry’s Disease Fabry’s Disease
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Leprosy Leprosy
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Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy
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Subacute Combined Degeneration Subacute Combined Degeneration
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Alcoholic Neuropathy Alcoholic Neuropathy
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Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis
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Management Management
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Suggested Reading Suggested Reading
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Cite
Low, Phillip A., 'Autonomic Neuropathies', Neurobiology of Disease, 2 edn (New York , 2016; online edn, Oxford Academic, 1 Mar. 2017), https://doi.org/10.1093/med/9780199937837.003.0118, accessed 4 May 2025.
Abstract
Autonomic neuropathy is a peripheral neuropathy with selective or disproportionate involvement of autonomic fibers. Because autonomic nerves innervate all organ systems, the manifestations of dysautonomia are protean. There are many causes of the autonomic neuropathies (Table 118.1). Some of the disorders in Table 118.1 are described in detail in other chapters. This chapter provides a brief description of the autonomic neuropathies, going from the acute/subacute to the more slowly evolving categories and finishing with some entities with less generalized dysautonomia.
Disclaimer
Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct.
Readers must therefore always …
More
Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct.
Readers must therefore always check the product information and clinical procedures with the most up to date published product information and data sheets
provided by the manufacturers and the most recent codes of conduct and safety regulations. The authors and the publishers do not accept responsibility or
legal liability for any errors in the text or for the misuse or misapplication of material in this work. Except where otherwise stated, drug dosages
and recommendations are for the non-pregnant adult who is not breastfeeding.
© Oxford University Press
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