Category: Genetic Disorders / Neurocutaneous Syndromes
Neurofibromatosis Type 2 (NF2) is a rare genetic disorder caused by a mutation in the NF2 gene, primarily characterized by bilateral vestibular schwannomas, leading to hearing loss, balance issues, and other neurological tumors.
Estimated at 1 in 25,000 to 1 in 40,000 live births worldwide (Source: Children's Tumor Foundation).
Discover the latest clinical trials and treatments for Neurofibromatosis Type 2 on JourneyForHealth.
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