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Hardback978-0-19-959001-8

£90.00February 2011

480 pp

The neuronal ceroid lipofuscinoses are an extremely rare group of inherited neurodegenerative diseases that primarily affect children. Core symptoms of these conditions typically include epilepsy, cognitive decline and visual failure. These diseases are so rare that professionals who come into contact with them need a consultative reference work that enables them to become expert, or identify who to contact for more details. Fully updated and revised, this second edition continues to be the definitive volume on this devastating group of disorders. Written by an international collection of authorities in the field, it provides invaluable advice on their diagnosis, patient care, and new treatments that are available.

This new edition of the definitive reference text on the neuronal ceroid lipofuscinoses will prove useful for clinicians, family physicians, research scientists, diagnostic laboratories, families affected by the disease as well as by workers in industry planning translational research.

· The definitive text on the Neuronal Ceroid Lipofuscinoses

· An updated, comprehensive volume on this devastating group of disorders

· Provides valuable advice on diagnosis, care, and new treatments

· Written by international authorities in the field

Edited by Sara Mole, MRC Laboratory for Molecular Cell Biology; Molecular Medicines Unit, UCL Institute of Child Health; and Department of Genetics, Evolution and Environment, University College London, UK, ruth WilliaMS, Evelina Children’s Hospital, Guy’s and St Thomas’ NHS Foundation Trust, London, UK and hanS Goebel, Professor of Neuropathology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany

The Neuronal Ceroid Lipofuscinoses (Batten Disease)

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