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NF1 is neurofibromatosis also has a variant NF2. NF1 affects 1 in 3000 people and isn't a disease, this is a condition which affects the nerves. Fibroma are small bumps which appear on nerve endings and can appear anywhere on the body. Signs of NF1 include cafe au lait patches which may be confused with birthmarks, feckled arm pits and groin area and neurofibroma. This conditon is not as well known as many other conditions like MS. This condition like all other have different serverites. Joesph Merrick (The Elephant Man) was at first thought to suffer from this but later rediagnosed. This can be passed on from parents to offspring. If either parent has this there is a 50/50 chance of passing it on to the child. THIS CONDITION IS NOT CONTAGIOUS and must not be treated or thought of as such.
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 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.
What are genetic disorders that involve more than one defective gene?
Some examples of genetic disorders involving more than one defective gene are cystic fibrosis, which is caused by mutations in the CFTR gene and other modifier genes; and certain types of neurofibromatosis, which result from mutations in both the NF1 and NF2 genes. These disorders demonstrate the complexity of genetic inheritance and the interactions between multiple genes.
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.
Your daughter is 7 year old she has nf1 she has neurofiborma on one of the eye nerve and spinal she also has dyslexia is nf1 and dyslexia related?
I amd 29 and I have NF1, I have read before that dyslexia is more common in nf1 patents, I was never officialy diagnosec. But I do have many of the signs of it. My mother does as well(she carried the NF1 Gene) If you would like to contact me about any other experences email me at samo333@hotmail.com and put NF1 in hte subject line.
Is epilepsy relative to nf1?
No.
Is neurofibromatosis occrs in India?
yes !! I suffer from NF1
How long do people live with nf1?
Individuals with Neurofibromatosis type 1 (NF1) generally have a normal life expectancy. However, they may face an increased risk of certain health issues, such as tumors, learning disabilities, and cardiovascular problems, which can affect quality of life. Early diagnosis and management of associated complications can help improve outcomes. Regular medical care is essential for monitoring and addressing potential issues related to NF1.
What are facts about neurofibromatosis?
People who have NF1 may have very few neurofibromas, or they may have thousands throughout their bodies
How is NF1 diagnosed?
Neurofibromatosis type 1 (NF1) is primarily diagnosed through clinical evaluation based on established criteria, which include the presence of specific features such as café-au-lait spots, neurofibromas, freckling in the armpits or groin, and optic gliomas. Genetic testing can confirm the diagnosis by identifying mutations in the NF1 gene, but it is not always necessary for diagnosis. A healthcare provider typically assesses the patient's family history and physical symptoms to make a conclusive diagnosis.
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.
Is nf1 worse then nf2?
Neurofibromatosis type 1 (NF1) and type 2 (NF2) are distinct genetic disorders with different characteristics and complications. NF1 is generally more common and can lead to a variety of complications, including skin tumors, bone abnormalities, and a higher risk of certain cancers. NF2 primarily involves the development of bilateral vestibular schwannomas, which can lead to hearing loss and balance issues. Whether one is considered "worse" than the other can depend on individual circumstances and the specific complications experienced by patients.
Can a prenatal test detect neurofibromatosis?
Clinical genetic testing can confirm the presence of a mutation in the neurofibromatosis type 1 (NF1) gene. Prenatal testing for NF1 mutations is also possible using amniocentesis or chorionic villus sampling procedures. Genetic testing for neurofibromatosis type 2 (NF2) mutations is sometimes available but is accurate only in about 65 percent of those individuals tested.
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 and is it hereditary?
Neuro- means nerve, fibro-means fiber, oma- means tumor, -tosis means condition of. The entire word means soft tumors involving nerves including all nerves and nerve fibers. This is a genetic disorder. There are two forms: NF1 (90%) and NF1. This disease was once called von Recklinghausen disease, named after the man who first described it.
What do you do if you have Neurofibromatosis type you?
If you have Neurofibromatosis type 1 (NF1), it’s important to maintain regular check-ups with a healthcare provider experienced in managing the condition. They can monitor for complications and provide guidance on managing symptoms, such as skin tumors or learning challenges. Staying informed about NF1 and connecting with support groups can also be beneficial for emotional support and resources. Additionally, a healthy lifestyle, including regular exercise and a balanced diet, can contribute to overall well-being.
