NF1 (Neurofibromatosis Type 1)

Neurofibromatosis Type 1 (NF1) is a genetic disorder that affects how cells grow, leading to the development of tumors along nerves in the skin, brain, and spinal cord. It can cause skin changes like light spots called café-au-lait spots, small bumps called neurofibromas, and sometimes affects eyesight, learning, and bones. NF1 is inherited and varies in severity; some people have mild symptoms, while others may experience more significant health issues. Though it is a lifelong condition, many individuals live active lives with appropriate monitoring and management.