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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.
What is the difference between neurofibromatosis 1 and neurofibromatosis 2?
Neurofibromatosis 1 hyperpigmented macules (cafe au lait spots) nerve tumors types: cutaneous, subcutaneous and plexiform neurofibromas Optical tumors optic pathway gliomas and Lisch nodules (bumps on iris of the eye) Bony abnomralities dysplasias (malformations) of the eye socket, vertebrae Thinning of the long bone cortex Scoliosis can occur as well learning deficits yet large head size Increased rick of non nervous system cancers Neurofibromatosis 2 generally just schwannomas, meningomas and the occasional cataracts. Also they are both affected by different chromosomes... patients with NF1 has a mutation on the long arm of chromosome 17 while neurofibromatosis 2 has a mutation on chromosome 22.
What is the meaning of neurofibermatosis?
Neurofibromatosis is an autosomal dominant disorder, which means only one copy of the affected gene is needed for the disorder to develop.
Can you die from Neurofibromatosis?
yes you can just like any other disease. some cases are more severe than others. most people who have nf1 can live normal, healthy lives. if you have nf2, the more severe case, it may very well shorten your lifespan.
Who discovered neurofibromatosis type 1?
Von Recklinghausen
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.
What did Francis Collins discover?
He discovered genes causing cystic fibrosis, neurofibromatosis, and Huntington Chorea. (i would spell check this answer) please look to further references.
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.
Is there a cure for neurofibromatosis?
no, not yet, but they are working to find one!
