Neurofibromatosis type 1 - Symptoms and causes - Mayo Clinic
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 and groin.
Neurofibromatosis type I - Wikipedia
Neurofibromatosis type I (NF-1), or von Recklinghausen syndrome, is a complex multi-system human disorder caused by the mutation of neurofibromin 1 (NF-1). NF-1 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.
Neurofibromatosis Type 1 (NF1) - Johns Hopkins Medicine
Neurofibromatosis type 1 (also called Von Recklinghausen’s disease, Von Recklinghausen neurofibromatosis and peripheral NF) is one of the most commoninherited disorders and affects about one in every 3,000 people. NF1 ranges from mild to severe, and can cause more symptoms in some people than in others.
Neurofibromatosis Type 1 - StatPearls - NCBI Bookshelf
Aug 13, 2023 · Neurofibromatosis-1 (NF-1), or Von Recklinghausen disease, is one of the inheritable neurocutaneous disorders manifested by developmental changes in the nervous system, bones, and skin. It is an autosomal dominant disorder.
Neurofibromatosis type 1 - MedlinePlus
Neurofibromatosis type 1 is a condition characterized by changes in skin coloring (pigmentation) and the growth of tumors along nerves in the skin, brain, and other parts of the body. Explore symptoms, inheritance, genetics of this condition.
Neurofibromatosis: What It Is, Symptoms, Types & Treatment
Nov 20, 2023 · There are three types of neurofibromatosis: Neurofibromatosis type 1 (NF1): NF1 is the most common type. It causes café au lait spots, nerve tumors (neurofibromas), armpit and groin freckles, eye nerve tumors and bone deformities (scoliosis).
Neurofibromatosis Type 1 (NF1): Symptoms & Treatment - Cleveland Clinic
May 1, 2024 · Neurofibromatosis type 1 (NF1) is the most common form of neurofibromatosis. It affects your skin and nervous system. Common symptoms include multiple café au lait spots and tumors in your skin and on your nerves.
Neurofibromatosis type 1 - Diagnosis and treatment - Mayo Clinic
To diagnose neurofibromatosis type 1 (NF1), a healthcare professional begins with a review of your personal and family medical history and a physical exam. Your child's skin is checked for cafe au lait spots, which can help diagnose NF1.
Neurofibromatosis type 1 - Children's Hospital of Philadelphia
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 - NHS
Neurofibromatosis type 1 (NF1) is a genetic condition that causes tumours to grow along your nerves. The tumours are usually non-cancerous and so usually cause only mild symptoms.