Cerebellar Disorders in Children – Chapter 24: Autosomal Dominant Spinocerebellar Ataxias (ebook)

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Chapter 24 – Autosomal Dominant Spinocerebellar Ataxias

Andrea H. Nemeth

This chapter addresses dominant ataxias seen in children that are not covered in the sections on leukodystrophies and metabolic disorders. The common terminology of spinocerebellar ataxias (SCA’s) is somewhat confusing: strictly speaking there should be evidence of impairment of the spinocerebellar tracts in addition to the cerebellum itself. Of course one of the most common types is Friedreich ataxia but we do not use the term SCA’s for this condition; generally speaking, SCA’s has come to be used for autosomal dominant ataxias, usually degenerative, irrespective of the underlying pathology.

Please note that Chapters 23-29 are also available in Part 5: Genetic and Metabolic Disorders.

About the Complete Book:

This clinically orientated text by an international group of experts is the first definitive reference book on disorders of the cerebellum in children. It presents a wealth of practical clinical experience backed up by a strong scientific basis for the information and guidance given. The first part sets out the theoretical underpinnings of cerebellar disorders. This is followed by sections on clinical conditions grouped according to common characteristics such as aetiology and symptomatology. The descriptions of the clinical conditions each systematically cover, as appropriate, epidemiology, prevalence, diagnostic criteria, clinical features (including course and prognosis), pathophysiology, genetics, investigations, differential diagnosis, and management and treatment. This book will be an invaluable resource for all those caring for children affected by cerebellar disorders, including malformations, genetic and metabolic disorders, acquired cerebellar damage, vascular disorders and acute ataxias. This comprehensive reference text on cerebellar disorders in children includes chapters on cerebellar development, prenatal cerebellar imaging, imaging of the posterior fossa, with coverage of a broad range of malformations, genetic and metabolic disorders involving the cerebellum, prenatal cerebellar disruptions (as related to prematurity), vascular disorders, tumors and paraneoplastic syndromes, as well as acute ataxia and trauma to the posterior fossa. Numerous checklists are provided to assist in the differential diagnosis of clinical signs and neuroimaging findings.

Readership 
Paediatric neurologists, paediatricians, neurologists, developmental paediatricians, neuroimaging specialists, geneticists, neonatologists

Clinics in Developmental Medicine No. 191-192