Affiliation:
1. Department of Radiotherapy, King George Medical University, Lucknow, Uttar Pradesh, India
Abstract
AbstractNeurofibromatosis type 2 (NF2) is also known as multiple inherited schwannomas, meningiomas, and ependymomas (MISME) syndrome. Mutation in NF2 gene is the cause for MISME syndrome. We are reporting here a case of MISME syndrome with triple tumor in a 30-year-old male patient who presented with the chief complaints of spastic paraparesis, bowel and bladder incontinence, and decreased vision in the right eye.
Subject
Oncology,Pediatrics, Perinatology and Child Health
Cited by
1 articles.
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