What is Neurofibromatosis Type 1 (NF1)?

The video discusses neurofibromatosis type 1 (NF1), a genetic condition causing nerve lumps. It covers the causes, symptoms, diagnosis, and management of NF1. Key symptoms include skin patches and lumps, while complications can involve learning difficulties, bone issues, and more. Regular checkups and a healthcare team are crucial for managing NF1. Emotional support and online groups can help those affected. Despite no cure, many with NF1 can lead fulfilling lives with proper care.

What is the primary cause of Neurofibromatosis Type 1?

• A bacterial infection

• An autoimmune disorder

• A change in genes

• A viral infection

Which of the following is a common skin sign of NF1?

• Red rashes

• Café au Lait spots

• White spots

• Blue patches

What type of neurofibroma is generally harmless?

• Plexiform neurofibromas

• Cutaneous neurofibromas

• Subcutaneous neurofibromas

• Intramuscular neurofibromas

Which of the following is NOT a potential complication of NF1?

• High blood pressure

• Diabetes

• Epilepsy

• Learning difficulties

Why is it important to have regular check-ups for NF1?

• To prevent the condition from spreading

• To ensure the condition is cured

• To monitor for new or changing symptoms

• To avoid any medical treatment