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.
How many chromosome numbers are affected with a person with neurofibromatosis.
The person credited with the discovery of neurofibromatosis is Fredich Daniel van Recklinghausen. He released an article identifying it back in 1882.
There are no available treatments for the disorders which underlie either type of neurofibromatosis. To some extent, the symptoms of NF-1 and NF-2 can be treated individually. Skin tumors can be surgically removed. Some brain tumors.
Mony Yassir _degrassi gillian andersond brother
chromosome.
Most girls are born with two X chromosomes, but girls with Turner syndrome are born with only one X chromosome or they are missing part of one X chromosome. The effects of the condition vary widely among girls with Turner syndrome. It all depends on how many of the body's cells are affected by the changes to the X chromosome.
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.
http://en.wikipedia.org/wiki/Neurofibromatosis
It's the X-chromosome, so whichever number corresponds to it.
Chromosome 22 contains about 693 genes. Some are:gene to produce immunoglobulingene to make neurofilamentsgene for light chains of antibodiesDamaged genes can cause:Schizophreniabilateral acoustic neuroma (hearing loss)22q13 deletion syndrome (autism)Breast canceramyotrophic lateral sclerosis (ALS)neurofibromatosis
Neurofibromatosis is usually diagnosed when the patient has 10 or more cafe-au-lait spots.
Yes, in Dallas, Texas it is called the NSG (Neurofibromatosis Support Group)
I found this useful link http://www.ninds.nih.gov/disorders/neurofibromatosis/neurofibromatosis.htm
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.
no, not yet, but they are working to find one!
yes !! I suffer from NF1