Neurofibromatosis is usually diagnosed when the patient has 10 or more cafe-au-lait spots.
WOW!! That guy is amazing. A chicken? Histerical, Neurofibromatosis affects only chromosome number 23. It also will affect the brain and is an autosomal dominant genetic disorder.It is when your chromosome has a chicken.
The genotype for Neurofibromatosis is typically inherited in an autosomal dominant pattern, caused by mutations in the NF1 gene located on chromosome 17. Individuals with Neurofibromatosis usually have a mutation in one copy of the NF1 gene.
Yes, there are support groups for neurofibromatosis. The Children's Tumor Foundation, NF Network, and NF Australia are some organizations that offer support and resources for individuals and families affected by neurofibromatosis. These groups provide opportunities for connections, information sharing, and emotional support.
Every one idiot
Neurofibromatosis - is a genetic condition... nota communicable disease. You cannot 'catch' it from a sufferer by way of intercourse with an affected person.
The NHS website has detailed information on neurofibromatosis. They have details of the diagnosis, causes, symptoms and possible treatments for the condition.
Neurofibromatosis was first described in medical literature in the late 1800s by Friedrich Daniel von Recklinghausen, a German pathologist. He characterized the condition and it was later named after him as Von Recklinghausen's disease or neurofibromatosis type 1 (NF1).
no, not yet, but they are working to find one!
yes !! I suffer from NF1
hard
Von Recklinghausen