First off---There are many different forms of Neurofibromatosis. Each type manifests itself in a different manner. NF1 being the most common. A good sign that your child MAY have NF1 is the visible sign of cafe au lait spots on the surface of the skin (they look like very light coloured birthmarks will appear at birth or shortly after (most people can have 1 or 2)--children with NF will have more than 5 (over 5cm in size). Children with NF1 may also have freckling under their armpits and around the groin area, a slightly larger head circumference, short stature, learning disabilities, freckling in the coloured part of their eyes, and small fleshy tumors may develop during puberty. This is only a really quick overview of NF1---to be completely sure you should see a family doctor(or one familiar with NF). NF testing is also a possibility if you suspect (or if their is a family history).---Please be reassured that NF is very diverse and affects EVERYONE in a different way---
If both parents have neurofibromatosis, the chances of their child inheriting the condition depend on the specific type of neurofibromatosis and the genetic patterns involved. For neurofibromatosis type 1 (NF1) and type 2 (NF2), which are both autosomal dominant disorders, there is a 25% chance the child will inherit the condition from each parent. If both parents have the same type, the likelihood of having a child with the disorder is higher, potentially leading to more severe manifestations. However, genetic counseling is recommended for specific risk assessment.
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.
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.
The NHS website has detailed information on neurofibromatosis. They have details of the diagnosis, causes, symptoms and possible treatments for the condition.
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.
no, not yet, but they are working to find one!
yes !! I suffer from NF1