Abstract
Other names: central neurofibromatosis; bilateral acoustic neurofibromatosis; bilateral acoustic neurinoma; bilateral acoustic schwannomas. Inheritance: autosomal dominant with almost complete penetrance; frequency is 3/10 newborns; neomutation represent 50% of cases; variable expressivity from mild disease through life (Gardner type) to severe condition at young age (Wishart type: with more than 3 tumours).
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