Genetic counselling – Childhood Tumour Trust

Return to course: Recognising Neurofibromatosis Type 1 Childhood Tumour Trust

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Recognising Neurofibromatosis Type 1

Pre-learning Reflection and Module Summary

What is Neurofibromatosis type 1
How common is NF1
What causes NF1?

Recognition of neurofibromatosis type 1 and referral
Typical symptoms - café-au-lait spots
Typical symptoms - unusual freckling
Typical symptoms - cutaneous and subcutaneous neurofibromas
Typical symptoms – plexiform neurofibromas
Other common signs and symptoms of NF1
Complications associated with NF1
The importance of recognising NF1
Diagnosing NF1
How is NF1 managed?
Genetic counselling
Advising parents and newly-diagnosed adults
Key points – recognising and referring for NF1

Assessment Questions

Post-learning reflection Questionairre

References
Resources

Feedback Questions

Genetic counselling

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