Neurofibromatosis Type 2 (NF2) - Johns Hopkins Medicine
NF2 is a neurologic disorder resulting from a change in the gene of the same name, the NF2 gene. When working properly, the NF2 gene prevents tumors from forming. In people with NF2, this gene is impaired and creates a greater risk of developing certain tumors.
Neurofibromatosis type 2 | About the Disease | GARD - Genetic …
Neurofibromatosis type 2 (NF2) is a disorder characterized by the growth of noncancerous tumors of the nervous system. Childhood symptoms include skin growths and eye findings. Almost all people with NF2 develop vestibular schwannomas affecting both ears.
Neurofibromatosis type 2 - MedlinePlus
Neurofibromatosis type 2 is a disorder characterized by the growth of noncancerous tumors in the nervous system. Explore symptoms, inheritance, genetics of this condition.
Neurofibromatosis Type 2 - StatPearls - NCBI Bookshelf
2022年10月3日 · Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder characterized by the development of multiple tumors involving the central nervous system (CNS). Bilateral vestibular schwannomas are the hallmark feature of NF2 and are present in approximately 90 to 95 percent of patients.
Neurofibromatosis Type 2 Clinic - Overview - Mayo Clinic
2024年7月9日 · Neurofibromatosis type 2 (NF2) is an uncommon genetic condition that results in the development of multiple brain tumors and spinal tumors. Almost all people with NF2 have two tumors affecting each of the hearing nerves, called vestibular schwannomas.
Neurofibromatosis Type 2 (NF2) - Cleveland Clinic
2023年11月16日 · NF2-related schwannomatosis, formerly known as neurofibromatosis type 2 (NF2), is a genetic condition that affects your nervous system. A genetic change tells your body to overproduce cells that form tumors.
NF2-Related Schwannomatosis - Symptoms, Causes, Treatment
2023年2月10日 · NF2-related schwannomatosis (NF2; previously known as neurofibromatosis 2) is a rare genetic disorder that is primarily characterized by noncancerous (benign) tumors of the nerves that transmit balance and sound impulses from the inner ears to the brain (bilateral acoustic neuromas/vestibular schwannomas).
Neurofibromatosis 1 and 2: Symptoms, Treatments, Causes - WebMD
2022年4月26日 · Neurofibromatosis is a genetic disorder of the nervous system which causes tumors to form on your nerve tissues. It causes multiple patches of tan or light brown skin and soft, fleshy growths...
Causes and Treatment of Neurofibromatosis Type 2 (NF2)
2024年3月27日 · Neurofibromatosis type 2 (NF2) is an uncommon genetic disorder that causes different types of benign tumors in the nervous system. Symptoms include tinnitus, hearing loss, and unsteadiness. NF2 is an autosomal dominant disorder that you can inherit from one parent.
Neurofibromatosis type 2 | Radiology Reference Article - Radiopaedia.org
2024年1月30日 · Neurofibromatosis type 2 (NF2) is a rare autosomal dominant neurocutaneous disorder (phakomatosis) manifesting as a development of multiple CNS tumors. Unlike neurofibromatosis type 1 (NF1), it is not associated with neurofibromas. Instead, patients with …
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