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Hate to break it to u... but no. It's 100 percent genetic, however it can be caused by spontaneous mutation. So you can get it from a parent, or through spontaneous mutation and that is when you get it out of your entire family. Not all NF cases are as severe though, my mom has it and it hasn't affected her at all except for the cafe au lait spots get a lot of questions. Of course... there can be downsides to it. My younger sis has it and as a result she has tumors on some nerve endings and has scoliosis. I may have it, but we don't know for sure. If I do it is the cause of my epilepsy. so no, unfortunately it cannot be prevented. but it is not always severe. I hope this helped!!!
What else can I help you with?
What chromosome does Neurofibromatosis effects?
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.
What is neurofibromatosis?
Neurofibromatosis is a genetic disorder that causes tumors to grow on nerves in various parts of the body. There are three types of neurofibromatosis: NF1, NF2, and schwannomatosis. Symptoms can vary widely and may include skin changes, hearing loss, and balance problems, depending on the type of neurofibromatosis. Treatment options focus on managing symptoms and monitoring for any potential complications.
Who discovered neurofibromatosis?
Neurofibromatosis was first formally described by the German pathologist Friedrich Daniel von Recklinghausen in the late 1800s. He published a detailed case study of the condition, which led to it being named after him as von Recklinghausen's disease.
Do any famous people have Neurofibromatosis?
Yes, actress Ashley Tisdale and American football player Matt Schobel have Neurofibromatosis. They have been open about their struggles with the condition, raising awareness and offering support to others facing similar challenges.
What is the cause of neorofibromatosis?
Neurofibromatosis is a genetic disorder caused by mutations in certain genes (NF1 and NF2) that are involved in controlling cell growth. It is usually inherited in an autosomal dominant pattern, meaning a person only needs one copy of the mutated gene to develop the condition. In some cases, it may also occur sporadically due to new mutations.
How can neurofibromatosis be diagnosed?
Neurofibromatosis is usually diagnosed when the patient has 10 or more cafe-au-lait spots.
What chromosome does Neurofibromatosis effects?
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.
What is the genotype for a person with the genetic disorder Neurofibromatosis?
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.
Are there any support groups for neurofibromatosis?
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.
Who does neurofibromatosis affect?
Every one idiot
Is neurofibromatosis tranferable threw intercourse?
Neurofibromatosis - is a genetic condition... nota communicable disease. You cannot 'catch' it from a sufferer by way of intercourse with an affected person.
Did Earnhardt have neurofibromatosis?
There is no public evidence to suggest that Dale Earnhardt had neurofibromatosis. Neurofibromatosis is a genetic disorder characterized by the growth of tumors on nerves, and while Earnhardt had various health concerns throughout his career, there has been no indication that he suffered from this specific condition. His death in a racing accident in 2001 was attributed to head injuries rather than any underlying medical condition like neurofibromatosis.
Where can a person go to find detailed information on neurofibromatosis?
The NHS website has detailed information on neurofibromatosis. They have details of the diagnosis, causes, symptoms and possible treatments for the condition.
When was neurofibromatosis discovered?
Neurofibromatosis type 1 (NF1) was first described in 1882 by the German pathologist Von Recklinghausen. Neurofibromatosis type 2 (NF2) was first described in 1820 by the Scottish surgeon JH Wishart.
Is there a cure for neurofibromatosis?
no, not yet, but they are working to find one!
Is neurofibromatosis occrs in India?
yes !! I suffer from NF1
What is everyday life like for a person with neurofibromatosis?
hard
