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Neuromuscular Disorders of Infancy, Childhood, and Adolescence

A Clinician's Approach

9780750671903
1 103,76 zł
993,38 zł Zniżka 110,38 zł Brutto
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Opis
Childhood neuromuscular disorders differ from adult diseases and require much experience to evaluate. However, most neurologists trained in EMG have little experience evaluating children or infants. This book, written by a stellar list of world-class experts in paediatric neuromuscular diseases, provides clinicians with the knowledge they need to successfully diagnose and treat their paediatric patients.
Szczegóły produktu
Butterworth-Heinemann
34551
9780750671903
9780750671903

Opis

Rok wydania
2002
Numer wydania
1
Oprawa
twarda
Liczba stron
1344
Wymiary (mm)
216 x 279
Waga (g)
3996
  • I. Clinical and Laboratory Approach to the Infant and Child with a Neuromuscular Problem
    1. Introduction: Historical Perspectives
    2. Genetics
    3. EMG
    4. Muscle Biopsy
    5. Nerve Biopsy


    II. Infantile Hypotonia and Arthrogryposis
    6. Neonatal Hypotonia
    7. Arthrogryposis


    III. Anterior Horn Cell Disorders
    8. Spinal Muscular Atrophies
    9. Juvenile Muscular Atrophy of Unilateral Upper Extremity (Hirayama Disease)
    10. Juvenile ALS vs. Other Motor Neuron Disorders
    11. Infantile Poliomyelitis and Other Enteropathic Motor Neuron Diseases


    IV. Radiculopathies and Plexopathies
    12. Radiculopathies
    13. Plexopathies Rabies


    Peripheral Nerve Disorders
    14. Vaccine Associated Poliomyelitis
    15. Tetanus
    16. Rabies


    Mononeuropathies
    17. Facial Palsies: Congenital and acquired
    18. Upper Extremities
    19. Lower Extremities


    Polyneuropathies
    20. Overview of the Neuropathies
    21. Congenital and Early Infantile Neuropathies
    22. Hereditary Charcot - Marie - Tooth and Other Genetic Neuropathies
    23. Guillain - Barre Syndrome
    24. Acute Moter Axonal Neuropathy in Childhood
    25. Tick Paralysis
    26. Chronic Inflammatory Demyelinating and Recurrent Neuropathies
    27. Peripheral Neuropathy in Inherited Metabolic Disease
    28. Neuropathies Secondary to Systemic Disorders
    29. Childhood Hansens Disease
    30. Toxic Neuropathies
    31. Autonomic Neuropathies


    V. Neuromuscular Junction Disorders
    32. Infantile Botulism
    33. Congential Miyasthenia Gravis
    34. Acquired Miyasthenia Gravis in Childhood


    VI. Myopathies
    35. Clinical Syndromes of Congenital Myopathies
    36. Congenital Muscular Dystrophies
    37. Dystrophinopathies
    38. Facioscapulohumeral Dystrophy, Scapuloperoneal Syndromes and Distal Myopathies
    39. The Limb Girdle Muscular Dystrophies
    40. Emery - Dreifuss Muscular Dystrophy
    41. Myopathies of Systemic Disease
    42. Channelopathies Affecting Skeletal Muscle in Childhood
    43. Glycogen Storage Diseases of Muscle
    44. Lipid Storage Muscular Disorders
    45. Myoadenylate Deaminase Deficiency
    46. Metabolic : Mitochondrial
    47. Juvenile Dermatomyositis and other Inflammatory Myopathies in Children
    48. Other Inflammatory Myopathies: Viral Trichinosis, and Pyomyositis
    49. Rigid Spine Syndromes


    VII. Special Clinical Problems
    50. Neuromuscular Problems of the Critically III Neonate and Child
    51. HyperCKemia and Rhabdomyolysis
    52. Malignant Hyperthermia
    53. Continuous Muscle Fiber Activity Including the Stiff Person
    54. Disorder of the Ocular Motor Cranial Nerves and Extraocular Muscles
    55. Neurogenic Dysphagia in Newborns and Infants
    56. Friedreichs Ataxis, Vitamin E. Deficiency
    57. Dominantly Inherited Spinocerebellar Syndromes
    58. Reflex Sympathetic Dystrophy


    VIII. General Therapeutic Principles
    59. Autoimmune Pharmacotherapeutic Intervention in Children
    60. Androgen and Corticosteroid Therapy of Muscular Dystrophies: New Therapeutic Modalities
    61. The Principles and Practice of Molecular Therapies
    62. Intensive Care Management
    63. Orthopedic Treatment
    64. Rehabilitation of the Pediatric Patient with a Neuromuscular Disease
    65. Bioethical Issues
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