Of the 156 IA patients, another five had symptoms suggestive of NF1: however, one had clinical features and histological findings indicative of schwannomatosis; two had a confirmed diagnosis of neurofibromatosis type 2 (NF2); one had features indicative of NF2; and one had a suspected neurofibroma that turned out to be a leiomyoma. The gene discussed is NF2; the disease is neurofibroma.