Diagnosing neurofibromatosis type 1 – Childhood Tumour Trust

Return to course: Recognising Neurofibromatosis Type 1 Childhood Tumour Trust

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Recognising Neurofibromatosis Type 1

Pre-learning Reflection

Neurofibromatosis type 1 is a genetic disorder
Neurofibromatosis type 1 is an autosomal dominant genetic condition
Manifestations of neurofibromatosis type 1

Recognition of neurofibromatosis type 1 and referral
Recognition and referral - café-au-lait spots
Recognition and referral - freckling and neurofibromas
Body mapping
Diagnosing neurofibromatosis type 1
How is neurofibromatosis type 1 managed?
Genetic counselling when planning a family
Key points in the recognition and referral of NF1

Assessment Questions

Post-learning reflection Questionairre

References
Resources for parents & carers

Feedback Questions

Diagnosing neurofibromatosis type 1

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