Understanding neurodegenerative disorders
Abstract
The clinical features that suggest a neurodegenerative process are first discussed, then frameworks for conceptualizing the disorders and constructing a differential diagnosis. The characteristic clinical features and the focused investigation of two groups of disorders are discussed: leukoencephalopathies and the neuronal ceroid lipofuscinoses. These are exemplars for the investigation of white and grey matter disorders, respectively. Lastly, the gangliosidoses and mucopolysaccharidoses are briefly discussed. These four groups of disorders constitute the most common neurodegenerative disorders in the United Kingdom.
Keywords: heredodegenerative disorders, nervous system, paediatrics, leukodystrophy, neuronal ceroid lipofuscinosis, gangliosidoses, mucopolysaccharidosis
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- f1 Correspondence to RS. Tel.: +44 (0)20 7837 7618; Fax: +44 (0)20 7833 9469; E-mail: r.surtees@ich.ucl.ac.uk
PII: S0957-5839(01)90283-0
doi:10.1054/cupe.2001.0283
© 2002 Elsevier Science Ltd. All rights reserved.

