The Dystonias is a new title introduced under the Contemporary Neurology Series defining the key features of one of the most frequently misdiagnosed of all movement disorders. This volume provides a comprehensive practical clinical resource that addresses how to recognize the many types of dystonia, how they are diagnosed and evaluated, and the currently available medical and surgical treatments. The dystonias are a heterogeneous group of disorders characterized by excessive muscle contractions leading to abnormal postures and movements. The clinical manifestations of dystonias are quite varied. The dystonias may emerge at any age from infancy through late adulthood, they may affect muscles in nearly any region of the body alone or in various combinations, they may occur without other clinical problems, or they may be combined with other neurological or systemic disorders. There aremany causes for dystonia too, both acquired and inherited. The chapters explore the clinical manifestations and causes which are quite varied for all age groups. Among adults, the most common syndromes affect a single body region such as the neck (cervical dystonia or torticollis), craniofacial region(blepharospasm or oromandibular dystonia), one limb (writers cramp or foot dystonia), the larynx (laryngeal dystonia or spasmodic dysphonia), or another region. For adults, most cases are idiopathic, and a cause cannot be found despite extensive workup. For children, dystonia often spreads to involve a broader region of the body, and a cause is more likely to be discovered. The most common syndromes among children include cerebral palsy or genetic disorders where dystonia may occur inisolation or combined with other clinical problems. The Dystonias will be the most useful guide for both pediatric and adult neurologists, as well as specialists in rehabilitation medicine or physiotherapy. This book will also be valuable for neurosurgeons, ophthalmologists, otolaryngologists, developmentalists, rehab specialists and physiotherapists.
Chapter 1: A brief history of the concept of dystonia and its evolution; Chapter 2: The defining clinical features of dystonia; Chapter 3: Classification and diagnostic strategy for dystonia; Chapter 4: Epidemiology of the dystonias; Chapter 5: Cervical dystonias; Chapter 6: Craniofacial dystonias; Chapter 7: Laryngeal dystonias; Chapter 8: Limb dystonias; Chapter 9: Isolated generalized dystonias; Chapter 10: Musicians and other task-specific dystonias; Chapter 11: Non-motor features of dystonia; Chapter 12: Dystonia and tremor; Chapter 13: Dystonia and parkinsonism; Chapter 14: Dystonia and ataxia; Chapter 15: Dystonia and myoclonus; Chapter 16: Dystonia and cerebral palsy; Chapter 17: Dystonia and the paroxysmal dyskinesias; Chapter 18: Dystonias combined with other features; Chapter 19: Dystonia induced by medications, illicit drugs, and environmental toxins; Chapter 20: Dystonia and trauma; Chapter 21: Dystonia and autoimmunity; Chapter 22: Dystonia genetics; Chapter 23: The neuroanatomical substrates of dystonia; Chapter 24: Dystonia physiology; Chapter 25: Psychogenic (functional) dystonia; Chapter 26: Pseudodystonia and differential diagnosis; Chapter 27: Workup of dystonia; Chapter 28: Symptom-targeted oral medications for dystonia; Chapter 29: Special interventions for certain types of dystonia; Chapter 30: Botulinum toxin treatment for dystonia; Chapter 31: Surgical treatments for dystonia; Chapter 32: Physiotherapy and complementary medicine for dystonia;
Komentarze (0)
Chwilowo nie możesz polubić tej opinii
Zgłoś komentarz
Czy jesteś pewien, że chcesz zgłosić ten komentarz?
Zgłoszenie wysłane
Twój komentarz został wysłany i będzie widoczny po zatwierdzeniu przez moderatora.