That is the information related to neurofibromatosis which is classified as a rare disease. Hopefully this information is useful.

A rare genetic disorder known as Neurofibromatosis type one, or NF1, affects about one in 2,500 people in the U.S.

Medically reviewed by Brigid Dwyer, MDMedically reviewed by Brigid Dwyer, MD Neurofibromatosis (NF) is a genetic neurological condition that is usually inherited. There are three types of ...

Cruz Hernandez will travel to Washington DC with his mother Maria Alvarado to advocate for Medical after struggle with rare disease Neurofibromatosis type 1 (NF1).

Gomekli (mirdametinib) is the first treatment that is FDA approved for both adults and children with neurofibromatosis ... up to 24 cycles or until their disease worsened or they had side effects ...

But for certain, the future will be filled with love. Enriquez lives with chronic kidney disease, neurofibromatosis, which causes tumors to form, scoliosis and Raynaud's phenomenon, causing ...

Given its varied manifestation among individuals, Neurofibromatosis Type 1 (NF1), a genetic condition reportedly affecting one in every 3,000 people worldwide, has prompted health experts to ...

Adult and pediatric patients with neurofibromatosis type 1 who have ... to the urgent need for treatments targeting rare pediatric diseases. The approval process was further expedited by the ...

Indonesian children with Neurofibromatosis Type 1 (NF1), a rare genetic condition where tumors grow on the nerves and skin, ...