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Journal of Child Neurology
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Reviews

Review Article : Neurofibromatosis 1: Clinical Review and Exceptions to the Rules

Helen Young, MBBS

Neurogenetics Research Unit Children's Hospital at Westmead, Division of Paediatrics and Child Health, University of Sydney, Sydney, Australia

Shelley Hyman, BSc Psych Hons

Kathryn North, MBBS Hons, MD, FRACP

Neurogenetics Research Unit Children's Hospital at Westmead, Division of Paediatrics and Child Health, University of Sydney, Sydney, Australia

Neurofibromatosis 1 is an autosomal dominant, multisystem disorder with myriad clinical manifestations. Between 1991 and 1998, 495 adults and children were diagnosed with neurofibromatosis 1 at a specialized neurogenetics clinic in Sydney, Australia. This review establishes the prevalence of the clinical manifestations of neurofibromatosis 1 in these patients and provides guidelines for assessment and management. In addition, we review in detail patients who had unusual presentations and who represent important "exceptions to the rules" of clinical practice. (J Child Neurol 2002;17:613-621).

Journal of Child Neurology, Vol. 17, No. 8, 613-621 (2002)
DOI: 10.1177/088307380201700812
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