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NEW EDITION
The Neuronal Ceroid Lipofuscinoses
(Batten Disease)
Second Edition
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
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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
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.
Hardback
978-0-19-959001-8
£90.00
February 2011
480 pp
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.
Please see overleaf for ordering details...
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