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Neurofibromatosis Type 1 in Childhood (International Review of Child Neurology (Mac Keith Press)) [Hardcover]

Bruce R. Korf , Kathryn North , David Gutman , Peter G. Procopis

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Book Description

29 May 1997 1898683131 978-1898683131
A great deal is now known about neurofibromatosis type 1, particularly as a result of the identification of its causative gene by positional cloning. Effective treatments for its resulting cosmetic disfigurement, impaired cognitive performance and even life-threatening malignancy however sadly remain elusive. As Dr Korf remarks in his Foreword; 'this book's cogent and thorough description of neurofibromatosis in children will take its place alongside other major clinical studies of the disorder. (Dr North) has tackled some of the more challenging issues, such as the basis for learning disabilities and the optimal means for early detection of optic gliomas. Her work provides a guide to the clinician and stands as a provocative challenge to the neurofibromatosis research community to further explore the basis of these problems.'

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Review

'It is a well written thesis which contains an updated review of the literature of the subject and underscores the author's expertise in neurofibromatosis … is to be recommended to paediatricians, neurologists and ophthalmologists interested in neurofibromatosis.' J. J. De Laey, Oogheelkunde, Universiteit Gent

'Any doctor who is involved in the management of children with NF1 will find this book useful.' Evan Reid, Journal of Medical Genetics

' … a very readable book that provides a wealth of information'. Doody's Health Sciences Book Review Journal

Book Description

Neurofibromatosis type 1, although genetically well defined, lacks effective treatments for its symptoms of disfigurement, cognitive impairment and numerous malignancies. Dr North both carefully describes its epidemiology and addresses some of these more challenging clinical issues. She provides a valuable guide to the clinician and a thoughtful read for the researcher.

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First Sentence
Neurofibromatosis type 1 (NF1) is a multisystem disorder with a prevalence of 1 in 4000 people (Huson et al. 1988). Read the first page
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