Doctor insights on:
Neurofibromatosis Type 2
Possible: NIH diagnostic criteria for NF1 with two or more of following features:1)6 or more café-au-lait macules over 5 mm in diameter prepubertal individuals over 15 mm in greatest diameter in postpubertal..2) 2or more neurofibromas or one plexiform neurofibroma.3)Freckling in armpit or groin areas4)Optic glioma (optic nerve tumor)5) > 2 Lisch nodules(iris of eye)6)typical bone lesions 7)1deg relative nf1 ...Read moreSee 1 more doctor answer
Neurofibromatosis: It depends on how severely affected the patient is with the disorder. The earlier the diagnosis and the most number of lesions and location (particularly in the spine and brain) diagnosed can affect how long someone will live. In my practice I have adults doing well in the midlife yet have lost patients to the disorder as teenagers so it is very variable. ...Read moreSee 1 more doctor answer
Shortened: Life expectancy for people with NF-2 is generally shortened compared to non-affected and NF-1 affected people, but it is also highly dependent on a number of potential conditions, and available treatments. I've added a link that is more comprehensive, and I hope it helps. http://www.ctf.org/pdf/brochures/NF2_Info_for_Patients_Families.pdf ...Read moreSee 2 more doctor answers
My sister has NEUROFIBROMATOSIS type 2. She only has the cafe spots on her body. Will I develop it too? Is there a chance she will get a tumor? :(
Depends on parent: NF2 inherited as change in the NF2 gene from one of parents. Some people have mutation with NF2 gene in first person in family to be affected. No matter if NF2 gene change was inherited from a parent or is newly affected, every person who has NF2 gene change has a 50% chance of passing on to children. If your parent does not have gene your sister was mutation and you are unlikely to have nf2. ...Read moreSee 1 more doctor answer
NO : Tow distinct gene mutations. Neurofibroma nf i & nf ii are both inhirted tppe i will show cutaneous, neurological and ortho malformations.Tend to be non cancerous nf ii is less frequent ( i in 40000 ) less skin lesions more neuroligical tumors, like maningiomas, bil aucoatic neuromas, schiwanomas, gliomas is part of misme syndrome. ...Read moreSee 2 more doctor answers
What to do if I have neurofibromatosis but I ain't show if it's type 1 of type 2 does anyone know how 2 find out?
Physician for help: Neurofibromatosis,inherited,with varying involvement from mild to severe.Neurofibroma is benign tumor that originates from the nerve cells.Tumors usually arise from nerves in or under skin.Type1 usually appears in children with brown flat skin spots, freckling in armpits, and soft tumors under skin and sometimes bone deformity.Type 2 usually brain tumors,vestibular schwannomas,acoustic neuromas. ...Read moreSee 1 more doctor answer
NF 1 is caused by : mutations of the NF gene, 17q11.2. Clinical course varies widely depending largely on location & size of brain, skin, eye & other tumors. Initial evaluations by a geneticist, ped. neurologist, ped. ophthalmologist, developmental/behavioral pediatrician. & Early Intervention, http://www.dds.ca.gov/EarlyStart/home.cfm., guide management. Learning Disabilities & ADHD are common. See www.ctf.org. ...Read more
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