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SECTIONS:
preface & acknowledgements
genetics at a glance
contacts, support & testing
testing & pregnancy
newborn screening
cancer in the family
cardiovascular conditions
chromosomal conditions
clotting & bleeding conditions
cystic fibrosis
diabetes
fragile X syndrome and other causes of developmental delay
haemoglobinopathies
hereditary haemochromatosis
neurofibromatosis
neurological conditions
psychiatric conditions
genetics in practice
emerging genetic technologies
glossary
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Neurofibromatosis
Neurofibromatosis type 1 (NF1)
GP's role
Clinical features
Genetics
Prevalence
Investigations
Management
Neurofibromatosis type 2 (NF2)
GP's role
Clinical features
Genetics
Prevalence
Investigations
Management
Implications for other family members
Bibliography