What is NF1? Neurofibromatosis type 1 (also called Von Recklinghausen’s disease, Von Recklinghausen neurofibromatosis and peripheral NF) is one of the most commoninherited …

Neurofibromatosis type 1 (NF1) is a genetic condition that causes changes in skin pigment and tumors on nerve tissue. Skin changes include flat, light brown spots and freckles in the armpits …

NF1 is a gene on chromosome 17 that is responsible for production of a protein (neurofibromin) which is needed for normal function in many human cell types. NF-1 causes tumors along the …

This condition is caused by genetic changes (DNA variants) in the NF1 gene and is inherited in an autosomal dominant pattern. NF1 is diagnosed based on a clinical examination, the specific …

Neurofibromatosis type 1 (NF1) is a genetic disorder characterized by the presence of skin differences. Ten percent of people with NF1 develop cancerous neurofibromas.

Neurofibromatosis type 1 (NF1) is a type of neurofibromatosis, which is a condition that affects your skin and nervous system (brain, spinal cord and nerves). NF1 affects how often certain …

Mutations in the NF1 gene cause neurofibromatosis type 1. The NF1 gene provides instructions for making a protein called neurofibromin. This protein is produced in many cells, including …

Learn all about Neurofibromatosis Type 1 (NF1) symptoms, diagnosis challenges, and the lifelong specialized care needed.

Neurofibromatosis type 1 (NF1) is a genetic condition where tumors (mostly benign) grow on skin, nerves, and bones. It is also known as von Recklinghausen disease.

Aug 18, 2024 · NF1 is caused by problems with a gene for a protein called neurofibromin. NF1 causes tissue along the nerves to grow uncontrollably. This growth can put pressure on …