Neuromuscular disease

Neuromuscular disease: a case-based approach

by Wokke, John H. J.

Type Book
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"There are over 600 neuromuscular disorders and the variability of these syndromes can leave clinicians feeling as if they are lost in a maze as they seek to diagnose and manage patients. This book addresses this problem by using the case-history and symptom manifestation as a starting point for the diagnostic process in adult patients, mimicking the situation in the consultation room. For each case, diagnostic tools, disease pathogenesis, prognosis and treatment options are discussed, along wi…

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Title Statements

  • Full title :Neuromuscular disease : a case-based approach / John H.J. Wokke [and others].

Summary

"There are over 600 neuromuscular disorders and the variability of these syndromes can leave clinicians feeling as if they are lost in a maze as they seek to diagnose and manage patients. This book addresses this problem by using the case-history and symptom manifestation as a starting point for the diagnostic process in adult patients, mimicking the situation in the consultation room. For each case, diagnostic tools, disease pathogenesis, prognosis and treatment options are discussed, along with rare manifestations and differential diagnoses. Symptoms, signs and syndromes are cross-linked to help the reader navigate the variety of disorders. Accompanying tables give a broader picture of the manifestations of a particular disease within the landscape of neuromuscular disorders. This highly-illustrated book, with accompanying videos, will aid neurologists at all levels, internists, geneticists, rehabilitation physicians and researchers in the field, as they seek to familiarize themselves with this complex range of disorders"--Provided by publisher.

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Edition Statements

  • Publication Date:2013.

Publication Statements

The Physical Object

  • Description:1 online resource

Edition Identifiers

  • ISBN:9781107336148, 1107336147, 9780511735905, 0511735901, 9781107332829, 1107332826, 9781107334489, 1107334489
  • oclc:ocn828628173
  • LC Classification:RC350.4
  • Dewey Decimal:616.8

Table of Contents

Introduction: approach to the patient -- Part I. Motor neurone diseases. Case 1. Classical amyotrophic lateral sclerosis ; Case 2. ALS with frontotemporal dementia ; Case 3. Primary lateral sclerosis ; Case 4. Progressive muscular atrophy ; Case 5. Kennedy disease ; Case 6. Spinal muscular atrophy type III, Kugelberg-Welander disease ; Case 7. Post-polio syndrome ; Case 8. Spinal dural fistula -- Part II. Neuropathies. Case 9. Charcot-Marie-Tooth disease type 1A ; Case 10. Hereditary neuropathy with liability to pressure palsy ; Case 11. Charcot-Marie-Tooth disease type 2A, mitofusinopathy ; Case 12. X-linked Charcot-Marie-Tooth disease ; Case 13. Hereditary sensory and autonomic neuropathy type 4 ; Case 14. Guillain-Barre; syndrome ; Case 15. Miller-Fisher syndrome ; Case 16. Chronic inflammatory demyelinating polyneuropathy ; Case 17. Multifocal motor neuropathy ; Case 18. Peripheral nerve hyperexcitability syndrome, Morvan's syndrome ; Case 19. Vasculitic neuropathy ; Case 20. Neuropathy and ataxia caused by IgM gammopathy ; Case 21. Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes ; Case 22. Subacute sensory paraneoplastic neuropathy and ganglionopathy …

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