Return to course: Recognising Neurofibromatosis Type 1 Childhood Tumour Trust

Recognising Neurofibromatosis Type 1

Introduction

Pre-learning Reflection

What is Neurofibromatosis Type 1?

Neurofibromatosis type 1 is a genetic disorder

Neurofibromatosis type 1 is an autosomal dominant genetic condition

Manifestations of neurofibromatosis type 1

Recognition of Neurofibromatosis

Recognition of neurofibromatosis type 1 and referral

Recognition and referral - café-au-lait spots

Recognition and referral - freckling and neurofibromas

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

Assessment Questions

Post-learning reflection

Post-learning reflection Questionairre

References and further reading

Feedback

Neurofibromatosis type 1 is an autosomal dominant genetic condition

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